Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190388181G= , CM000665.2:g.190388181G= | GRCh38 |
| NC_000003.11:g.190105970G= , CM000665.1:g.190105970G= | GRCh37 |
| NC_000003.10:g.191588664G= | NCBI36 |
| NG_008149.1:g.5130G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.3:c.-149G= MANE Select | ENSP00000264734.3:n.-149G= | |
| ENST00000456423.2:c.-149G= | ENSP00000414136.2:n.-149G= | |
| ENST00000264734.2:c.62G= | ENSP00000264734.2:p.Arg21= | |
| ENST00000456423.1:c.62G= | ENSP00000414136.1:p.Arg21= | |
| ENST00000468220.1:n.306+13578G= | ||
| NM_006580.3:c.62G= | NP_006571.1:p.Arg21= | |
| NM_001378492.1:c.-93-56G= | NP_001365421.1:n.-93-56G= | |
| NM_001378493.1:c.-93-56G= | NP_001365422.1:n.-93-56G= | |
| NM_006580.4:c.-149G= MANE Select | NP_006571.2:n.-149G= |