Linked Data
MyVariant Identifiers:
chr20:g.44640232C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46011593C>T , CM000682.2:g.46011593C>T | GRCh38 |
| NC_000020.10:g.44640232C>T , CM000682.1:g.44640232C>T | GRCh37 |
| NC_000020.9:g.44073639C>T | NCBI36 |
| NG_011468.1:g.7686C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000372330.3:c.843C>T MANE Select | ENSP00000361405.3:p.Gly281= | |
| NM_004994.2:c.843C>T | NP_004985.2:p.Gly281= | |
| NM_004994.3:c.843C>T MANE Select | NP_004985.2:p.Gly281= |