Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50130525C= , CM000676.2:g.50130525C= | GRCh38 |
| NC_000014.8:g.50597243C= , CM000676.1:g.50597243C= | GRCh37 |
| NC_000014.7:g.49666993C= | NCBI36 |
| NG_051073.1:g.106169G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216373.10:c.3313G= MANE Select | ENSP00000216373.5:p.Asp1105= | |
| ENST00000216373.9:c.3313G= | ENSP00000216373.5:p.Asp1105= | |
| ENST00000543680.5:c.3214G= | ENSP00000445328.1:p.Asp1072= | |
| NM_006939.2:c.3313G= | NP_008870.2:p.Asp1105= | |
| XM_005268021.1:c.3133G= | XP_005268078.1:p.Asp1045= | |
| XM_011537103.1:c.3274G= | XP_011535405.1:p.Asp1092= | |
| NM_006939.3:c.3313G= | NP_008870.2:p.Asp1105= | |
| NM_006939.4:c.3313G= MANE Select | NP_008870.2:p.Asp1105= |