Linked Data
MyVariant Identifiers:
chr19:g.18898442C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18787633C>T , CM000681.2:g.18787633C>T | GRCh38 |
| NC_000019.9:g.18898442C>T , CM000681.1:g.18898442C>T | GRCh37 |
| NC_000019.8:g.18759442C>T | NCBI36 |
| NG_007070.1:g.8673G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.993G>A MANE Select | ENSP00000222271.2:p.Val331= | |
| ENST00000222271.6:c.993G>A | ENSP00000222271.2:p.Val331= | |
| ENST00000425807.1:c.834G>A | ENSP00000403792.1:p.Val278= | |
| ENST00000542601.6:c.894G>A | ENSP00000439156.2:p.Val298= | |
| NM_000095.2:c.993G>A | NP_000086.2:p.Val331= | |
| NM_000095.3:c.993G>A MANE Select | NP_000086.2:p.Val331= |