Linked Data
dbSNP Id:
rs2135847586
gnomAD v3:
12-120997532-G-T
gnomAD v4:
12-120997532-G-T
MyVariant Identifiers:
chr12:g.121435335G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.120997532G>T , CM000674.2:g.120997532G>T | GRCh38 |
| NC_000012.11:g.121435335G>T , CM000674.1:g.121435335G>T | GRCh37 |
| NC_000012.10:g.119919718G>T | NCBI36 |
| NG_011731.2:g.23787G>T , LRG_522:g.23787G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000560968.6:c.*115G>T | ENSP00000453965.2:n.*115G>T | |
| ENST00000257555.11:c.1368G>T MANE Select | ENSP00000257555.5:p.Leu456= | |
| ENST00000257555.10:c.1368G>T | ENSP00000257555.4:p.Leu456= | |
| ENST00000400024.6:c.1368G>T | ENSP00000476181.1:p.Leu456= | |
| ENST00000402929.5:n.2234G>T | ||
| ENST00000535955.5:n.84G>T | ||
| ENST00000538626.2:n.232G>T | ||
| ENST00000538646.5:c.*344G>T | ENSP00000443964.1:n.*344G>T | |
| ENST00000540108.1:c.*808G>T | ENSP00000445445.1:n.*808G>T | |
| ENST00000541395.5:c.1368G>T | ENSP00000443112.1:p.Leu456= | |
| ENST00000541924.5:c.*382G>T | ENSP00000440361.1:n.*382G>T | |
| ENST00000543255.1:n.412G>T | ||
| ENST00000543427.5:c.831G>T | ENSP00000439721.2:p.Leu277= | |
| ENST00000544413.2:c.1368G>T | ENSP00000438804.1:p.Leu456= | |
| ENST00000544574.5:c.*131G>T | ENSP00000438565.1:n.*131G>T | |
| ENST00000560968.5:c.1185G>T | ||
| ENST00000615446.4:c.156G>T | ENSP00000483994.1:p.Leu52= | |
| ENST00000617366.4:c.587-102G>T | ENSP00000481967.1:n.587-102G>T | |
| NM_000545.5:c.1368G>T , LRG_522t1:c.1368G>T | NP_000536.5:p.Leu456= | |
| NM_000545.6:c.1368G>T | NP_000536.5:p.Leu456= | |
| NM_001306179.1:c.1368G>T | NP_001293108.1:p.Leu456= | |
| XM_005253931.2:c.1368G>T | XP_005253988.1:p.Leu456= | |
| XM_024449168.1:c.1368G>T | XP_024304936.1:p.Leu456= | |
| NM_000545.8:c.1368G>T MANE Select | NP_000536.6:p.Leu456= | |
| NM_001306179.2:c.1368G>T | NP_001293108.2:p.Leu456= |