Linked Data
MyVariant Identifiers:
chr13:g.33629278A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.33055141A>T , CM000675.2:g.33055141A>T | GRCh38 |
| NC_000013.10:g.33629278A>T , CM000675.1:g.33629278A>T | GRCh37 |
| NC_000013.9:g.32527278A>T | NCBI36 |
| NG_011485.1:g.43708A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380099.4:c.1425A>T MANE Select | ENSP00000369442.3:p.Gly475= | |
| ENST00000380099.3:c.1425A>T | ENSP00000369442.3:p.Gly475= | |
| ENST00000487852.1:n.1433A>T | ||
| NM_004795.3:c.1425A>T | NP_004786.2:p.Gly475= | |
| XM_006719895.1:c.504A>T | XP_006719958.1:p.Gly168= | |
| XM_006719895.2:c.504A>T | XP_006719958.1:p.Gly168= | |
| NM_004795.4:c.1425A>T MANE Select | NP_004786.2:p.Gly475= |