Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7496053G>T , CM000679.2:g.7496053G>T | GRCh38 |
| NC_000017.10:g.7399372G>T , CM000679.1:g.7399372G>T | GRCh37 |
| NC_000017.9:g.7340096G>T | NCBI36 |
| NG_027747.1:g.16675G>T | |
| NG_027747.2:g.16675G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000937.5:c.206G>T MANE Select | NP_000928.1:p.Gly69Val |
| NM_000937.4:c.206G>T | NP_000928.1:p.Gly69Val |
| ENST00000572844.1:c.206G>T | ENSP00000461879.1:p.Gly69Val |
| ENST00000617998.4:c.206G>T | ENSP00000480158.1:p.Gly69Val |
| ENST00000617998.6:n.605G>T | |
| ENST00000621442.4:c.206G>T | ENSP00000483957.1:p.Gly69Val |
| ENST00000674977.2:c.206G>T | ENSP00000502190.2:p.Gly69Val |