Canonical Allele Identifier:
CA205140039
Gene:
MyVariant.info:
GRCh38
chr10:g.29047920G>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.29047920G>T , CM000672.2:g.29047920G>T | GRCh38 |
| NC_000010.10:g.29336849G>T , CM000672.1:g.29336849G>T | GRCh37 |
| NC_000010.9:g.29376855G>T | NCBI36 |