Canonical Allele Identifier: CA200504718
Gene:

Linked Data

dbSNP Id: rs911454742
MyVariant Identifiers: chr9:g.129654538C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129654538C>G , CM000671.2:g.129654538C>G GRCh38
NC_000009.11:g.132416817C>G , CM000671.1:g.132416817C>G GRCh37
NC_000009.10:g.131456638C>G NCBI36