Canonical Allele Identifier: CA163625046

Gene:

Linked Data

• dbSNP Id: rs368670426
• MyVariant Identifiers: chr7:g.97017830A>T (hg19) ; chr7:g.97388518A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97388518A>T , CM000669.2:g.97388518A>T	GRCh38
NC_000007.13:g.97017830A>T , CM000669.1:g.97017830A>T	GRCh37
NC_000007.12:g.96855766A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001745293.1:n.127-59871T>A