Canonical Allele Identifier: CA863579145

Gene:

Linked Data

• ClinVar Variation Id: 1440985
• ClinVar RCV Id: RCV001978990
• dbSNP Id: rs1206526864
• MyVariant Identifiers: chr9:g.35658105A>G (hg19) ; chr9:g.35658108A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658108A>G , CM000671.2:g.35658108A>G	GRCh38
NC_000009.11:g.35658105A>G , CM000671.1:g.35658105A>G	GRCh37
NC_000009.10:g.35648105A>G	NCBI36
NG_017041.1:g.4911T>C , LRG_163:g.4911T>C
NG_033120.1:g.4819A>G