Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17018896C>T , CM000663.2:g.17018896C>T | GRCh38 |
| NC_000001.10:g.17345391C>T , CM000663.1:g.17345391C>T | GRCh37 |
| NC_000001.9:g.17217978C>T | NCBI36 |
| NG_012340.1:g.40275G>A , LRG_316:g.40275G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.657G>A | ENSP00000481376.2:p.Lys219= | |
| ENST00000491274.6:c.786G>A | ENSP00000480482.2:p.Lys262= | |
| ENST00000375499.8:c.828G>A MANE Select | ENSP00000364649.3:p.Lys276= | |
| ENST00000375499.7:c.828G>A | ENSP00000364649.3:p.Lys276= | |
| ENST00000475049.5:n.253G>A | ||
| ENST00000485092.5:n.492G>A | ||
| NM_003000.2:c.828G>A , LRG_316t1:c.828G>A | NP_002991.2:p.Lys276= | |
| NM_003000.3:c.828G>A MANE Select | NP_002991.2:p.Lys276= |