Linked Data
MyVariant Identifiers:
chr10:g.17849650G>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17849650G>T , CM000672.2:g.17849650G>T | GRCh38 |
| NG_047011.1:g.45308G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000569591.3:c.1135G>T MANE Select | ENSP00000455897.1:p.Asp379Tyr | |
| ENST00000569591.2:c.1135G>T | ENSP00000455897.1:p.Asp379Tyr | |
| NM_002438.3:c.1135G>T | NP_002429.1:p.Asp379Tyr | |
| NM_002438.4:c.1135G>T MANE Select | NP_002429.1:p.Asp379Tyr |