Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38071141C= , CM000664.2:g.38071141C= | GRCh38 |
| NC_000002.11:g.38298284C= , CM000664.1:g.38298284C= | GRCh37 |
| NC_000002.10:g.38151788C= | NCBI36 |
| NG_008386.2:g.9961G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000490576.2:c.1213G= | ENSP00000478839.2:p.Ala405= | |
| ENST00000610745.5:c.1213G= MANE Select | ENSP00000478561.1:p.Ala405= | |
| ENST00000492443.1:n.591G= | ||
| ENST00000494864.1:c.100G= | ENSP00000479876.1:p.Ala34= | |
| ENST00000610745.4:c.1213G= | ENSP00000478561.1:p.Ala405= | |
| ENST00000614273.1:c.1213G= | ENSP00000483678.1:p.Ala405= | |
| NM_000104.3:c.1213G= | NP_000095.2:p.Ala405= | |
| NM_000104.4:c.1213G= MANE Select | NP_000095.2:p.Ala405= |