Canonical Allele Identifier: CA834982466

Gene:

Linked Data

• dbSNP Id: rs1288168373
• MyVariant Identifiers: chr7:g.148258016A>T (hg19) ; chr7:g.148560924A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.148560924A>T , CM000669.2:g.148560924A>T	GRCh38
NC_000007.13:g.148258016A>T , CM000669.1:g.148258016A>T	GRCh37
NC_000007.12:g.147888949A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_928099.1:n.300+7176T>A
XR_928100.1:n.433+7176T>A