Linked Data
MyVariant Identifiers:
chr19:g.18896887T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18786077T>A , CM000681.2:g.18786077T>A | GRCh38 |
| NC_000019.9:g.18896887T>A , CM000681.1:g.18896887T>A | GRCh37 |
| NC_000019.8:g.18757887T>A | NCBI36 |
| NG_007070.1:g.10228A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.1377A>T MANE Select | ENSP00000222271.2:p.Ser459= | |
| ENST00000222271.6:c.1377A>T | ENSP00000222271.2:p.Ser459= | |
| ENST00000425807.1:c.1218A>T | ENSP00000403792.1:p.Ser406= | |
| ENST00000542601.6:c.1278A>T | ENSP00000439156.2:p.Ser426= | |
| NM_000095.2:c.1377A>T | NP_000086.2:p.Ser459= | |
| NM_000095.3:c.1377A>T MANE Select | NP_000086.2:p.Ser459= |