Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612314A= , CM000679.2:g.41612314A= | GRCh38 |
| NC_000017.10:g.39768566A= , CM000679.1:g.39768566A= | GRCh37 |
| NC_000017.9:g.37022092A= | NCBI36 |
| NG_008301.1:g.5514T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301653.9:c.375T= MANE Select | ENSP00000301653.3:p.Asn125= | |
| ENST00000301653.8:c.375T= | ENSP00000301653.3:p.Asn125= | |
| ENST00000588319.1:n.452T= | ||
| ENST00000593067.1:c.-312-28T= | ENSP00000467124.1:n.-312-28T= | |
| NM_005557.3:c.375T= | NP_005548.2:p.Asn125= | |
| NM_005557.4:c.375T= MANE Select | NP_005548.2:p.Asn125= |