Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160121223G>T , CM000663.2:g.160121223G>T | GRCh38 |
| NC_000001.10:g.160091013G>T , CM000663.1:g.160091013G>T | GRCh37 |
| NC_000001.9:g.158357637G>T | NCBI36 |
| NG_008014.1:g.10466G>T , LRG_6:g.10466G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000702.4:c.149G>T MANE Select | NP_000693.1:p.Gly50Val |
| ENST00000361216.8:c.149G>T MANE Select | ENSP00000354490.3:p.Gly50Val |
| NM_000702.3:c.149G>T | NP_000693.1:p.Gly50Val |
| ENST00000361216.7:c.149G>T | ENSP00000354490.3:p.Gly50Val |
| ENST00000392233.7:c.149G>T | ENSP00000376066.3:p.Gly50Val |
| ENST00000472488.5:n.252G>T | |
| ENST00000478587.1:n.429G>T |