Canonical Allele Identifier:
CA192563038
Gene:
MyVariant.info:
GRCh38
chr9:g.31419917G>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.31419917G>T , CM000671.2:g.31419917G>T | GRCh38 |
| NC_000009.11:g.31419915G>T , CM000671.1:g.31419915G>T | GRCh37 |
| NC_000009.10:g.31409915G>T | NCBI36 |