Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134842225G>T , CM000671.2:g.134842225G>T | GRCh38 |
| NC_000009.11:g.137734071G>T , CM000671.1:g.137734071G>T | GRCh37 |
| NC_000009.10:g.136873892G>T | NCBI36 |
| NG_008030.1:g.205420G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000093.5:c.5439G>T MANE Select | NP_000084.3:p.Val1813= |
| ENST00000371817.8:c.5439G>T MANE Select | ENSP00000360882.3:p.Val1813= |
| NM_000093.4:c.5439G>T | NP_000084.3:p.Val1813= |
| NM_001278074.1:c.5439G>T | NP_001265003.1:p.Val1813= |
| NR_103451.2:n.71-22016C>A | |
| ENST00000371817.7:c.5439G>T | ENSP00000360882.3:p.Val1813= |
| ENST00000371820.4:c.5439G>T | ENSP00000360885.4:p.Val1813= |
| ENST00000618395.4:c.5439G>T | ENSP00000481360.1:p.Val1813= |