Linked Data
ClinVar Variation Id:
1576661
ClinVar RCV Id:
RCV002085489
dbSNP Id:
rs1874700949
gnomAD v4:
12-102843762-C-T
MyVariant Identifiers:
chr12:g.103237540C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102843762C>T , CM000674.2:g.102843762C>T | GRCh38 |
| NC_000012.11:g.103237540C>T , CM000674.1:g.103237540C>T | GRCh37 |
| NC_000012.10:g.101761670C>T | NCBI36 |
| NG_008690.1:g.78841G>A | |
| NG_008690.2:g.119649G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.1083G>A MANE Select | ENSP00000448059.1:p.Lys361= | |
| ENST00000307000.7:c.1068G>A | ENSP00000303500.2:p.Lys356= | |
| ENST00000549247.6:n.842G>A | ||
| ENST00000551114.2:n.745G>A | ||
| ENST00000553106.5:c.1083G>A | ENSP00000448059.1:p.Lys361= | |
| ENST00000635477.1:c.187G>A | ||
| ENST00000635528.1:n.598G>A | ||
| NM_000277.1:c.1083G>A | NP_000268.1:p.Lys361= | |
| XM_011538422.1:c.1026G>A | XP_011536724.1:p.Lys342= | |
| NM_000277.2:c.1083G>A | NP_000268.1:p.Lys361= | |
| NM_001354304.1:c.1083G>A | NP_001341233.1:p.Lys361= | |
| NM_000277.3:c.1083G>A MANE Select | NP_000268.1:p.Lys361= | |
| NM_001354304.2:c.1083G>A | NP_001341233.1:p.Lys361= |