Linked Data
ClinVar Variation Id:
2756662
ClinVar RCV Id:
RCV003566907
dbSNP Id:
rs145240086
gnomAD v2:
12-121431489-G-T
gnomAD v3:
12-120993686-G-T
gnomAD v4:
12-120993686-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.120993686G>T , CM000674.2:g.120993686G>T | GRCh38 |
| NC_000012.11:g.121431489G>T , CM000674.1:g.121431489G>T | GRCh37 |
| NC_000012.10:g.119915872G>T | NCBI36 |
| NG_011731.2:g.19941G>T , LRG_522:g.19941G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000560968.6:c.693G>T | ENSP00000453965.2:p.Thr231= | |
| ENST00000257555.11:c.693G>T MANE Select | ENSP00000257555.5:p.Thr231= | |
| ENST00000257555.10:c.693G>T | ENSP00000257555.4:p.Thr231= | |
| ENST00000400024.6:c.693G>T | ENSP00000476181.1:p.Thr231= | |
| ENST00000402929.5:n.828G>T | ||
| ENST00000535955.5:n.43-3805G>T | ||
| ENST00000538626.2:n.191-3805G>T | ||
| ENST00000538646.5:c.527-478G>T | ENSP00000443964.1:n.527-478G>T | |
| ENST00000540108.1:c.*133G>T | ENSP00000445445.1:n.*133G>T | |
| ENST00000541395.5:c.693G>T | ENSP00000443112.1:p.Thr231= | |
| ENST00000541924.5:c.693G>T | ENSP00000440361.1:p.Thr231= | |
| ENST00000543427.5:c.633+60G>T | ENSP00000439721.2:n.633+60G>T | |
| ENST00000544413.2:c.693G>T | ENSP00000438804.1:p.Thr231= | |
| ENST00000544574.5:c.73-2931G>T | ENSP00000438565.1:n.73-2931G>T | |
| ENST00000560968.5:c.836G>T | ||
| ENST00000615446.4:c.-257-2576G>T | ENSP00000483994.1:n.-257-2576G>T | |
| ENST00000617366.4:c.586+107G>T | ENSP00000481967.1:n.586+107G>T | |
| NM_000545.5:c.693G>T , LRG_522t1:c.693G>T | NP_000536.5:p.Thr231= | |
| NM_000545.6:c.693G>T | NP_000536.5:p.Thr231= | |
| NM_001306179.1:c.693G>T | NP_001293108.1:p.Thr231= | |
| XM_005253931.2:c.693G>T | XP_005253988.1:p.Thr231= | |
| XM_024449168.1:c.693G>T | XP_024304936.1:p.Thr231= | |
| NM_000545.8:c.693G>T MANE Select | NP_000536.6:p.Thr231= | |
| NM_001306179.2:c.693G>T | NP_001293108.2:p.Thr231= |