Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.186539566C= , CM000665.2:g.186539566C= | GRCh38 |
| NC_000003.11:g.186257355C= , CM000665.1:g.186257355C= | GRCh37 |
| NC_000003.10:g.187740049C= | NCBI36 |
| NG_009829.1:g.9813G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_017541.4:c.53G= MANE Select | NP_060011.1:p.Gly18= |
| ENST00000307944.6:c.53G= MANE Select | ENSP00000312099.5:p.Gly18= |
| NM_017541.2:c.53G= | NP_060011.1:p.Gly18= |
| NM_017541.3:c.53G= | NP_060011.1:p.Gly18= |
| ENST00000307944.5:c.53G= | ENSP00000312099.5:p.Gly18= |
| ENST00000392499.6:c.53G= | ENSP00000376287.2:p.Gly18= |
| ENST00000460288.1:n.955G= |