Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612316T>C , CM000679.2:g.41612316T>C | GRCh38 |
| NC_000017.10:g.39768568T>C , CM000679.1:g.39768568T>C | GRCh37 |
| NC_000017.9:g.37022094T>C | NCBI36 |
| NG_008301.1:g.5512A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005557.4:c.373A>G MANE Select | NP_005548.2:p.Asn125Asp |
| ENST00000301653.9:c.373A>G MANE Select | ENSP00000301653.3:p.Asn125Asp |
| NM_005557.3:c.373A>G | NP_005548.2:p.Asn125Asp |
| ENST00000301653.8:c.373A>G | ENSP00000301653.3:p.Asn125Asp |
| ENST00000588319.1:n.450A>G | |
| ENST00000593067.1:c.-312-30A>G | ENSP00000467124.1:n.-312-30A>G |