Linked Data
ClinVar Variation Id:
2912967
ClinVar RCV Id:
RCV003727603
dbSNP Id:
rs771320133
ExAC:
12:121432138 G / A
gnomAD v2:
12-121432138-G-A
gnomAD v3:
12-120994335-G-A
gnomAD v4:
12-120994335-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.120994335G>A , CM000674.2:g.120994335G>A | GRCh38 |
| NC_000012.11:g.121432138G>A , CM000674.1:g.121432138G>A | GRCh37 |
| NC_000012.10:g.119916521G>A | NCBI36 |
| NG_011731.2:g.20590G>A , LRG_522:g.20590G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000560968.6:c.750+135G>A | ENSP00000453965.2:n.750+135G>A | |
| ENST00000257555.11:c.885G>A MANE Select | ENSP00000257555.5:p.Pro295= | |
| ENST00000257555.10:c.885G>A | ENSP00000257555.4:p.Pro295= | |
| ENST00000400024.6:c.885G>A | ENSP00000476181.1:p.Pro295= | |
| ENST00000402929.5:n.1020G>A | ||
| ENST00000535955.5:n.43-3156G>A | ||
| ENST00000538626.2:n.191-3156G>A | ||
| ENST00000538646.5:c.698G>A | ENSP00000443964.1:p.Arg233Gln | |
| ENST00000540108.1:c.*325G>A | ENSP00000445445.1:n.*325G>A | |
| ENST00000541395.5:c.885G>A | ENSP00000443112.1:p.Pro295= | |
| ENST00000541924.5:c.713+629G>A | ENSP00000440361.1:n.713+629G>A | |
| ENST00000543427.5:c.633+709G>A | ENSP00000439721.2:n.633+709G>A | |
| ENST00000544413.2:c.885G>A | ENSP00000438804.1:p.Pro295= | |
| ENST00000544574.5:c.73-2282G>A | ENSP00000438565.1:n.73-2282G>A | |
| ENST00000560968.5:c.893+135G>A | ||
| ENST00000615446.4:c.-257-1927G>A | ENSP00000483994.1:n.-257-1927G>A | |
| ENST00000617366.4:c.586+756G>A | ENSP00000481967.1:n.586+756G>A | |
| NM_000545.5:c.885G>A , LRG_522t1:c.885G>A | NP_000536.5:p.Pro295= | |
| NM_000545.6:c.885G>A | NP_000536.5:p.Pro295= | |
| NM_001306179.1:c.885G>A | NP_001293108.1:p.Pro295= | |
| XM_005253931.2:c.885G>A | XP_005253988.1:p.Pro295= | |
| XM_024449168.1:c.885G>A | XP_024304936.1:p.Pro295= | |
| NM_000545.8:c.885G>A MANE Select | NP_000536.6:p.Pro295= | |
| NM_001306179.2:c.885G>A | NP_001293108.2:p.Pro295= |