Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38070949G= , CM000664.2:g.38070949G= | GRCh38 |
| NC_000002.11:g.38298092G= , CM000664.1:g.38298092G= | GRCh37 |
| NC_000002.10:g.38151596G= | NCBI36 |
| NG_008386.2:g.10153C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000104.4:c.1405C= MANE Select | NP_000095.2:p.Arg469= |
| ENST00000610745.5:c.1405C= MANE Select | ENSP00000478561.1:p.Arg469= |
| NM_000104.3:c.1405C= | NP_000095.2:p.Arg469= |
| ENST00000490576.2:c.1405C= | ENSP00000478839.2:p.Arg469= |
| ENST00000494864.1:c.292C= | ENSP00000479876.1:p.Arg98= |
| ENST00000610745.4:c.1405C= | ENSP00000478561.1:p.Arg469= |
| ENST00000614273.1:c.1405C= | ENSP00000483678.1:p.Arg469= |