Canonical Allele Identifier: CA860367850

Gene:

Linked Data

• dbSNP Id: rs1438718773
• MyVariant Identifiers: chr9:g.132339037C>T (hg19) ; chr9:g.129576758C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576758C>T , CM000671.2:g.129576758C>T	GRCh38
NC_000009.11:g.132339037C>T , CM000671.1:g.132339037C>T	GRCh37
NC_000009.10:g.131378858C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_930390.1:n.182+1160C>T