Canonical Allele Identifier: CA168906892

Gene:

Linked Data

• dbSNP Id: rs936733509
• MyVariant Identifiers: chr7:g.148257974T>C (hg19) ; chr7:g.148560882T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.148560882T>C , CM000669.2:g.148560882T>C	GRCh38
NC_000007.13:g.148257974T>C , CM000669.1:g.148257974T>C	GRCh37
NC_000007.12:g.147888907T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_928099.1:n.300+7218A>G
XR_928100.1:n.433+7218A>G