Canonical Allele Identifier: CA862161368

Gene:

Linked Data

• dbSNP Id: rs1463262873
• gnomAD v3: 9-21756107-C-A
• gnomAD v4: 9-21756107-C-A
• MyVariant Identifiers: chr9:g.21756106C>A (hg19) ; chr9:g.21756107C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21756107C>A , CM000671.2:g.21756107C>A	GRCh38
NC_000009.11:g.21756106C>A , CM000671.1:g.21756106C>A	GRCh37
NC_000009.10:g.21746106C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746563.2:n.163+11718G>T