Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.144474920G>T , CM000670.2:g.144474920G>T | GRCh38 |
| NC_000008.10:g.145700303G>T , CM000670.1:g.145700303G>T | GRCh37 |
| NC_000008.9:g.145671111G>T | NCBI36 |
| NG_030003.1:g.6416C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003923.3:c.416C>A MANE Select | NP_003914.1:p.Ala139Asp |
| ENST00000377317.5:c.416C>A MANE Select | ENSP00000366534.4:p.Ala139Asp |
| NM_003923.2:c.416C>A | NP_003914.1:p.Ala139Asp |
| ENST00000377317.4:c.416C>A | ENSP00000366534.4:p.Ala139Asp |
| ENST00000525197.1:n.445C>A |