Canonical Allele Identifier: CA200300469
Gene:

Linked Data

dbSNP Id: rs964391754
MyVariant Identifiers: chr9:g.127814826G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127814826G>C , CM000671.2:g.127814826G>C GRCh38
NC_000009.11:g.130577105G>C , CM000671.1:g.130577105G>C GRCh37
NC_000009.10:g.129616926G>C NCBI36
NG_009551.1:g.44943C>G , LRG_589:g.44943C>G
NG_023245.1:g.16952G>C