Linked Data
MyVariant Identifiers:
chr19:g.49564036T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.49060779T>G , CM000681.2:g.49060779T>G | GRCh38 |
| NC_000019.9:g.49564036T>G , CM000681.1:g.49564036T>G | GRCh37 |
| NC_000019.8:g.54255848T>G | NCBI36 |
| NG_016289.1:g.8089A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000599795.5:c.243+976A>C | ENSP00000470689.1:n.243+976A>C | |
| XM_011527575.1:c.-27A>C | XP_011525877.1:n.-27A>C | |
| XR_001753693.1:n.879+385A>C | ||
| XR_001753694.1:n.910A>C |