Linked Data
ClinVar Variation Id:
1776631
ClinVar RCV Id:
RCV002401089
dbSNP Id:
rs376537508
ExAC:
12:52306925 C / T
gnomAD v2:
12-52306925-C-T
gnomAD v3:
12-51913141-C-T
gnomAD v4:
12-51913141-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.51913141C>T , CM000674.2:g.51913141C>T | GRCh38 |
| NC_000012.11:g.52306925C>T , CM000674.1:g.52306925C>T | GRCh37 |
| NC_000012.10:g.50593192C>T | NCBI36 |
| NG_009549.1:g.10724C>T , LRG_543:g.10724C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000547400.6:c.146C>T | ENSP00000446724.2:p.Thr49Met | |
| ENST00000551576.6:c.104C>T | ENSP00000455848.2:p.Thr35Met | |
| ENST00000552678.2:c.104C>T | ENSP00000457394.2:p.Thr35Met | |
| ENST00000388922.9:c.104C>T MANE Select | ENSP00000373574.4:p.Thr35Met | |
| ENST00000388922.8:c.104C>T | ENSP00000373574.4:p.Thr35Met | |
| ENST00000419526.6:c.103+606C>T | ENSP00000392492.2:n.103+606C>T | |
| ENST00000547400.5:c.146C>T | ENSP00000446724.1:p.Thr49Met | |
| ENST00000550683.5:c.146C>T | ENSP00000447884.1:p.Thr49Met | |
| ENST00000551576.5:c.104C>T | ENSP00000455848.1:p.Thr35Met | |
| NM_000020.2:c.104C>T , LRG_543t1:c.104C>T | NP_000011.2:p.Thr35Met | |
| NM_001077401.1:c.104C>T | NP_001070869.1:p.Thr35Met | |
| XM_005269235.2:c.104C>T | XP_005269292.1:p.Thr35Met | |
| XM_011539008.1:c.146C>T | XP_011537310.1:p.Thr49Met | |
| NM_000020.3:c.104C>T MANE Select | NP_000011.2:p.Thr35Met | |
| NM_001077401.2:c.104C>T | NP_001070869.1:p.Thr35Met |