Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.39581162C= , CM000677.2:g.39581162C= | GRCh38 |
| NC_000015.9:g.39873363C= , CM000677.1:g.39873363C= | GRCh37 |
| NC_000015.8:g.37660655C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260356.6:c.-96C= MANE Select | ENSP00000260356.5:n.-96C= | |
| ENST00000260356.5:c.-96C= | ENSP00000260356.5:n.-96C= | |
| ENST00000397591.2:c.-217C= | ENSP00000380720.2:n.-217C= | |
| NM_003246.2:c.-96C= | NP_003237.2:n.-96C= | |
| NM_003246.3:c.-96C= | NP_003237.2:n.-96C= | |
| XM_011521970.1:c.-217C= | XP_011520272.1:n.-217C= | |
| XM_011521971.1:c.-96C= | XP_011520273.1:n.-96C= | |
| XR_931897.1:n.80C= | ||
| XM_011521971.2:c.-96C= | XP_011520273.1:n.-96C= | |
| NM_003246.4:c.-96C= MANE Select | NP_003237.2:n.-96C= |