Canonical Allele Identifier: CA862161366

Gene:

Linked Data

• dbSNP Id: rs1298504666
• MyVariant Identifiers: chr9:g.21756103G>T (hg19) ; chr9:g.21756104G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21756104G>T , CM000671.2:g.21756104G>T	GRCh38
NC_000009.11:g.21756103G>T , CM000671.1:g.21756103G>T	GRCh37
NC_000009.10:g.21746103G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746563.2:n.163+11721C>A