Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1213572A= , CM000667.2:g.1213572A= | GRCh38 |
| NC_000005.9:g.1213687A= , CM000667.1:g.1213687A= | GRCh37 |
| NC_000005.8:g.1266687A= | NCBI36 |
| NG_008282.1:g.16978A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304460.11:c.773A= MANE Select | ENSP00000305302.10:p.Asn258= | |
| ENST00000304460.10:c.773A= | ENSP00000305302.10:p.Asn258= | |
| ENST00000515652.5:c.681A= | ENSP00000425701.1:p.Gln227= | |
| NM_001003841.2:c.773A= | NP_001003841.1:p.Asn258= | |
| NM_001003841.3:c.773A= MANE Select | NP_001003841.1:p.Asn258= |