Canonical Allele Identifier: CA862568033

Gene:

Linked Data

• dbSNP Id: rs1469428240
• gnomAD v3: 9-25551193-A-G
• gnomAD v4: 9-25551193-A-G
• MyVariant Identifiers: chr9:g.25551191A>G (hg19) ; chr9:g.25551193A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551193A>G , CM000671.2:g.25551193A>G	GRCh38
NC_000009.11:g.25551191A>G , CM000671.1:g.25551191A>G	GRCh37
NC_000009.10:g.25541191A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929525.1:n.50-621T>C
XR_929525.2:n.674-621T>C