Linked Data
MyVariant Identifiers:
chr15:g.74755085T>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74755085T>G , CM000677.2:g.74755085T>G | GRCh38 |
| NG_008431.2:g.37544T>G | |
| NG_061543.1:g.11241T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.1548T>G MANE Select | ENSP00000342007.4:p.Asn516Lys | |
| ENST00000343932.4:c.1548T>G | ENSP00000342007.4:p.Asn516Lys | |
| NM_000761.4:c.1548T>G | NP_000752.2:p.Asn516Lys | |
| NM_000761.5:c.1548T>G MANE Select | NP_000752.2:p.Asn516Lys |