Linked Data
ClinVar Variation Id:
2942282
ClinVar RCV Id:
RCV003805496
MyVariant Identifiers:
chr12:g.13768580C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.13615646C>T , CM000674.2:g.13615646C>T | GRCh38 |
| NC_000012.11:g.13768580C>T , CM000674.1:g.13768580C>T | GRCh37 |
| NC_000012.10:g.13659847C>T | NCBI36 |
| NG_031854.1:g.369443G>A | |
| NG_031854.2:g.371367G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000609686.4:c.1347G>A MANE Select | ENSP00000477455.1:p.Glu449= | |
| ENST00000630791.2:c.1347G>A | ENSP00000486677.2:p.Glu449= | |
| ENST00000609686.3:c.1347G>A | ENSP00000477455.1:p.Glu449= | |
| NM_000834.3:c.1347G>A | NP_000825.2:p.Glu449= | |
| XM_011520628.1:c.1347G>A | XP_011518930.1:p.Glu449= | |
| XM_011520629.1:c.1347G>A | XP_011518931.1:p.Glu449= | |
| XM_011520630.1:c.1347G>A | XP_011518932.1:p.Glu449= | |
| XR_931372.1:n.307+420C>T | ||
| XR_931373.1:n.447+420C>T | ||
| XR_931374.1:n.246+420C>T | ||
| NM_000834.4:c.1347G>A | NP_000825.2:p.Glu449= | |
| XM_011520628.2:c.1347G>A | XP_011518930.1:p.Glu449= | |
| XM_011520629.2:c.1347G>A | XP_011518931.1:p.Glu449= | |
| XM_017019219.2:c.1347G>A | XP_016874708.1:p.Glu449= | |
| XR_001749013.1:n.728+420C>T | ||
| XR_931372.2:n.444+420C>T | ||
| XR_931373.2:n.586+420C>T | ||
| NM_000834.5:c.1347G>A MANE Select | NP_000825.2:p.Glu449= |