Linked Data
MyVariant Identifiers:
chr19:g.18896863G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18786053G>T , CM000681.2:g.18786053G>T | GRCh38 |
| NC_000019.9:g.18896863G>T , CM000681.1:g.18896863G>T | GRCh37 |
| NC_000019.8:g.18757863G>T | NCBI36 |
| NG_007070.1:g.10252C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1401C>A MANE Select | ENSP00000222271.2:p.Ala467= | |
| ENST00000222271.6:c.1401C>A | ENSP00000222271.2:p.Ala467= | |
| ENST00000425807.1:c.1242C>A | ENSP00000403792.1:p.Ala414= | |
| ENST00000542601.6:c.1302C>A | ENSP00000439156.2:p.Ala434= | |
| NM_000095.2:c.1401C>A | NP_000086.2:p.Ala467= | |
| NM_000095.3:c.1401C>A MANE Select | NP_000086.2:p.Ala467= |