Canonical Allele Identifier: CA76316047

Gene:

Linked Data

• dbSNP Id: rs950568828
• MyVariant Identifiers: chr3:g.61413735A>G (hg19) ; chr3:g.61428061A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.61428061A>G , CM000665.2:g.61428061A>G	GRCh38
NC_000003.11:g.61413735A>G , CM000665.1:g.61413735A>G	GRCh37
NC_000003.10:g.61388775A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_940892.1:n.165-375T>C
XR_940893.1:n.164+453T>C
XR_001740725.1:n.202+453T>C
XR_940892.2:n.203-375T>C