Canonical Allele Identifier: CA77246662

Gene:

Linked Data

• dbSNP Id: rs972706014
• MyVariant Identifiers: chr3:g.72315901A>T (hg19) ; chr3:g.72266750A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.72266750A>T , CM000665.2:g.72266750A>T	GRCh38
NC_000003.11:g.72315901A>T , CM000665.1:g.72315901A>T	GRCh37
NC_000003.10:g.72398591A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940958.1:n.835+8358T>A