Linked Data
ClinVar Variation Id:
2875848
ClinVar RCV Id:
RCV003626440
gnomAD v4:
12-4912485-C-T
MyVariant Identifiers:
chr12:g.5021651C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4912485C>T , CM000674.2:g.4912485C>T | GRCh38 |
| NC_000012.11:g.5021651C>T , CM000674.1:g.5021651C>T | GRCh37 |
| NC_000012.10:g.4891912C>T | NCBI36 |
| NG_011815.1:g.7579C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.1107C>T MANE Select | ENSP00000371985.3:p.Ser369= | |
| ENST00000543874.3:n.105+2013C>T | ||
| ENST00000639306.1:c.945C>T | ENSP00000492506.1:p.Ser315= | |
| ENST00000639680.1:c.76+219C>T | ||
| ENST00000382545.3:c.1107C>T | ENSP00000371985.3:p.Ser369= | |
| ENST00000541095.1:n.105+2013C>T | ||
| ENST00000543874.2:n.96+2013C>T | ||
| NM_000217.2:c.1107C>T | NP_000208.2:p.Ser369= | |
| NM_000217.3:c.1107C>T MANE Select | NP_000208.2:p.Ser369= |