Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154187949G= , CM000685.2:g.154187949G= | GRCh38 |
| NC_000023.10:g.153453438G= , CM000685.1:g.153453438G= | GRCh37 |
| NG_011606.1:g.10354G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000595290.6:c.292G= MANE Select | ENSP00000472316.1:p.Ala98= | |
| ENST00000595290.5:c.292G= | ENSP00000472316.1:p.Ala98= | |
| ENST00000595330.1:n.302G= | ||
| NM_000513.2:c.292G= MANE Select | NP_000504.1:p.Ala98= |