Linked Data
ClinVar Variation Id:
92842
dbSNP Id:
rs143105337
ExAC:
13:49050942 C / T
gnomAD v2:
13-49050942-C-T
gnomAD v3:
13-48476806-C-T
gnomAD v4:
13-48476806-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48476806C>T , CM000675.2:g.48476806C>T | GRCh38 |
| NC_000013.10:g.49050942C>T , CM000675.1:g.49050942C>T | GRCh37 |
| NC_000013.9:g.47948943C>T | NCBI36 |
| NG_009009.1:g.178060C>T , LRG_517:g.178060C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.2626C>T MANE Select | ENSP00000267163.4:p.Arg876Cys | |
| ENST00000643064.1:c.194+95363C>T | ||
| ENST00000650461.1:c.2626C>T | ENSP00000497193.1:p.Arg876Cys | |
| ENST00000267163.4:c.2626C>T | ENSP00000267163.4:p.Arg876Cys | |
| ENST00000484879.1:n.360C>T | ||
| ENST00000531171.5:n.229C>T | ||
| NM_000321.2:c.2626C>T , LRG_517t1:c.2626C>T | NP_000312.2:p.Arg876Cys | |
| XM_011535171.1:c.2365C>T | XP_011533473.1:p.Arg789Cys | |
| XM_011535171.2:c.2365C>T | XP_011533473.1:p.Arg789Cys | |
| NM_000321.3:c.2626C>T MANE Select | NP_000312.2:p.Arg876Cys |