Linked Data
MyVariant Identifiers:
chr19:g.18900080T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18789271T>A , CM000681.2:g.18789271T>A | GRCh38 |
| NC_000019.9:g.18900080T>A , CM000681.1:g.18900080T>A | GRCh37 |
| NC_000019.8:g.18761080T>A | NCBI36 |
| NG_007070.1:g.7035A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.417A>T MANE Select | ENSP00000222271.2:p.Arg139= | |
| ENST00000222271.6:c.417A>T | ENSP00000222271.2:p.Arg139= | |
| ENST00000425807.1:c.391-379A>T | ENSP00000403792.1:n.391-379A>T | |
| ENST00000542601.6:c.318A>T | ENSP00000439156.2:p.Arg106= | |
| NM_000095.2:c.417A>T | NP_000086.2:p.Arg139= | |
| NM_000095.3:c.417A>T MANE Select | NP_000086.2:p.Arg139= |