Linked Data
MyVariant Identifiers:
chr10:g.17849644C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17849644C>T , CM000672.2:g.17849644C>T | GRCh38 |
| NG_047011.1:g.45302C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000569591.3:c.1129C>T MANE Select | ENSP00000455897.1:p.His377Tyr | |
| ENST00000569591.2:c.1129C>T | ENSP00000455897.1:p.His377Tyr | |
| NM_002438.3:c.1129C>T | NP_002429.1:p.His377Tyr | |
| NM_002438.4:c.1129C>T MANE Select | NP_002429.1:p.His377Tyr |