Linked Data
MyVariant Identifiers:
chr19:g.49564130A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.49060873A>T , CM000681.2:g.49060873A>T | GRCh38 |
| NC_000019.9:g.49564130A>T , CM000681.1:g.49564130A>T | GRCh37 |
| NC_000019.8:g.54255942A>T | NCBI36 |
| NG_016289.1:g.7995T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599795.5:c.243+882T>A | ENSP00000470689.1:n.243+882T>A | |
| XM_011527575.1:c.-121T>A | XP_011525877.1:n.-121T>A | |
| XR_001753693.1:n.879+291T>A | ||
| XR_001753694.1:n.880-64T>A |