Linked Data
dbSNP Id:
rs1947356489
gnomAD v3:
12-4912167-T-C
gnomAD v4:
12-4912167-T-C
MyVariant Identifiers:
chr12:g.5021333T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4912167T>C , CM000674.2:g.4912167T>C | GRCh38 |
| NC_000012.11:g.5021333T>C , CM000674.1:g.5021333T>C | GRCh37 |
| NC_000012.10:g.4891594T>C | NCBI36 |
| NG_011815.1:g.7261T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.789T>C MANE Select | ENSP00000371985.3:p.Ile263= | |
| ENST00000543874.3:n.105+1695T>C | ||
| ENST00000639306.1:c.627T>C | ENSP00000492506.1:p.Ile209= | |
| ENST00000382545.3:c.789T>C | ENSP00000371985.3:p.Ile263= | |
| ENST00000541095.1:n.105+1695T>C | ||
| ENST00000543874.2:n.96+1695T>C | ||
| NM_000217.2:c.789T>C | NP_000208.2:p.Ile263= | |
| NM_000217.3:c.789T>C MANE Select | NP_000208.2:p.Ile263= |