Canonical Allele Identifier: CA862161279

Gene:

Linked Data

• dbSNP Id: rs1447331929
• MyVariant Identifiers: chr9:g.21755963T>C (hg19) ; chr9:g.21755964T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21755964T>C , CM000671.2:g.21755964T>C	GRCh38
NC_000009.11:g.21755963T>C , CM000671.1:g.21755963T>C	GRCh37
NC_000009.10:g.21745963T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746563.2:n.163+11861A>G