Linked Data
MyVariant Identifiers:
chr8:g.19809357T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19951846T>A , CM000670.2:g.19951846T>A | GRCh38 |
| NC_000008.10:g.19809357T>A , CM000670.1:g.19809357T>A | GRCh37 |
| NC_000008.9:g.19853637T>A | NCBI36 |
| NG_008855.1:g.17776T>A | |
| NG_008855.2:g.55130T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.327T>A MANE Select | ENSP00000497642.1:p.Ile109= | |
| ENST00000311322.8:c.327T>A | ENSP00000309757.6:p.Ile109= | |
| ENST00000520959.5:c.99T>A | ENSP00000428496.1:p.Ile33= | |
| ENST00000524029.5:c.327T>A | ENSP00000428237.1:p.Ile109= | |
| NM_000237.2:c.327T>A | NP_000228.1:p.Ile109= | |
| NM_000237.3:c.327T>A MANE Select | NP_000228.1:p.Ile109= |