Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.114785510C= , CM000671.2:g.114785510C= | GRCh38 |
| NC_000009.11:g.117547790C= , CM000671.1:g.117547790C= | GRCh37 |
| NC_000009.10:g.116587611C= | NCBI36 |
| NG_011488.2:g.25619G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000374045.5:c.*4942G= MANE Select | ENSP00000363157.3:n.*4942G= | |
| ENST00000374045.4:c.*4942G= | ENSP00000363157.3:n.*4942G= | |
| NM_001204344.1:c.5521G= | NP_001191273.1:n.5521G= | |
| NM_005118.3:c.*4942G= | NP_005109.2:n.*4942G= | |
| NM_005118.4:c.*4942G= MANE Select | NP_005109.2:n.*4942G= |