Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11965503C>G , CM000663.2:g.11965503C>G | GRCh38 |
| NC_000001.10:g.12025560C>G , CM000663.1:g.12025560C>G | GRCh37 |
| NC_000001.9:g.11948147C>G | NCBI36 |
| NG_008159.1:g.35815C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000196061.5:c.1494C>G MANE Select | ENSP00000196061.4:p.Asn498Lys | |
| ENST00000196061.4:c.1494C>G | ENSP00000196061.4:p.Asn498Lys | |
| ENST00000470133.1:n.108C>G | ||
| ENST00000491536.5:n.122C>G | ||
| NM_000302.3:c.1494C>G | NP_000293.2:p.Asn498Lys | |
| NM_001316320.1:c.1635C>G | NP_001303249.1:p.Asn545Lys | |
| XM_011541594.1:c.1575C>G | XP_011539896.1:p.Asn525Lys | |
| XM_024447707.1:c.828C>G | XP_024303475.1:p.Asn276Lys | |
| NM_000302.4:c.1494C>G MANE Select | NP_000293.2:p.Asn498Lys | |
| NM_001316320.2:c.1635C>G | NP_001303249.1:p.Asn545Lys |