Linked Data
MyVariant Identifiers:
chr10:g.94179013C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.92419256C>T , CM000672.2:g.92419256C>T | GRCh38 |
| NC_000010.10:g.94179013C>T , CM000672.1:g.94179013C>T | GRCh37 |
| NC_000010.9:g.94168993C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000430958.1:n.590C>T | ||
| NR_038243.2:n.596C>T |