Canonical Allele Identifier: CA586881659

Gene:

Linked Data

• dbSNP Id: rs1245062043
• gnomAD v2: 9-21756032-A-G
• gnomAD v3: 9-21756033-A-G
• gnomAD v4: 9-21756033-A-G
• MyVariant Identifiers: chr9:g.21756032A>G (hg19) ; chr9:g.21756033A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21756033A>G , CM000671.2:g.21756033A>G	GRCh38
NC_000009.11:g.21756032A>G , CM000671.1:g.21756032A>G	GRCh37
NC_000009.10:g.21746032A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746563.2:n.163+11792T>C