Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.58576740G= , CM000663.2:g.58576740G= | GRCh38 |
| NC_000001.10:g.59042412G= , CM000663.1:g.59042412G= | GRCh37 |
| NC_000001.9:g.58815000G= | NCBI36 |
| NG_016237.1:g.5755C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371225.4:c.417C= MANE Select | ENSP00000360269.2:p.Gly139= | |
| ENST00000371225.3:c.417C= | ENSP00000360269.2:p.Gly139= | |
| NM_002353.2:c.417C= | NP_002344.2:p.Gly139= | |
| NM_002353.3:c.417C= MANE Select | NP_002344.2:p.Gly139= |