Linked Data
ClinVar Variation Id:
1912919
ClinVar RCV Id:
RCV002593482
MyVariant Identifiers:
chr12:g.13906634C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.13753700C>T , CM000674.2:g.13753700C>T | GRCh38 |
| NC_000012.11:g.13906634C>T , CM000674.1:g.13906634C>T | GRCh37 |
| NC_000012.10:g.13797901C>T | NCBI36 |
| NG_031854.1:g.231389G>A | |
| NG_031854.2:g.233313G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000609686.4:c.627G>A MANE Select | ENSP00000477455.1:p.Leu209= | |
| ENST00000630791.2:c.627G>A | ENSP00000486677.2:p.Leu209= | |
| ENST00000609686.3:c.627G>A | ENSP00000477455.1:p.Leu209= | |
| NM_000834.3:c.627G>A | NP_000825.2:p.Leu209= | |
| XM_011520628.1:c.627G>A | XP_011518930.1:p.Leu209= | |
| XM_011520629.1:c.627G>A | XP_011518931.1:p.Leu209= | |
| XM_011520630.1:c.627G>A | XP_011518932.1:p.Leu209= | |
| NM_000834.4:c.627G>A | NP_000825.2:p.Leu209= | |
| XM_011520628.2:c.627G>A | XP_011518930.1:p.Leu209= | |
| XM_011520629.2:c.627G>A | XP_011518931.1:p.Leu209= | |
| XM_017019219.2:c.627G>A | XP_016874708.1:p.Leu209= | |
| NM_000834.5:c.627G>A MANE Select | NP_000825.2:p.Leu209= |