Linked Data
MyVariant Identifiers:
chr14:g.101349490T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.100883153T>G , CM000676.2:g.100883153T>G | GRCh38 |
| NC_000014.8:g.101349490T>G , CM000676.1:g.101349490T>G | GRCh37 |
| NC_000014.7:g.100419243T>G | NCBI36 |
| NG_045001.1:g.6695A>C | |
| NG_045000.5:g.51885T>G | |
| NG_045000.6:g.51885T>G | |
| NG_045001.2:g.25570A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649591.1:c.1636A>C MANE Select | ENSP00000497482.1:p.Arg546= | |
| ENST00000534062.1:c.1636A>C | ENSP00000435342.1:p.Arg546= | |
| NM_001134888.2:c.1636A>C | NP_001128360.1:p.Arg546= | |
| NM_001134888.3:c.1636A>C MANE Select | NP_001128360.1:p.Arg546= |