Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43755344A>T , CM000679.2:g.43755344A>T | GRCh38 |
| NC_000017.10:g.41832712A>T , CM000679.1:g.41832712A>T | GRCh37 |
| NC_000017.9:g.39188238A>T | NCBI36 |
| NG_008078.2:g.8445T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301691.3:c.640T>A MANE Select | ENSP00000301691.1:p.Ter214Lys | |
| ENST00000301691.2:c.640T>A | ENSP00000301691.1:p.Ter214Lys | |
| NM_025237.2:c.640T>A | NP_079513.1:p.Ter214Lys | |
| NM_025237.3:c.640T>A MANE Select | NP_079513.1:p.Ter214Lys |