Canonical Allele Identifier: CA162129256

Gene:

Linked Data

• dbSNP Id: rs887081392
• MyVariant Identifiers: chr7:g.87543120G>A (hg19) ; chr7:g.87913805G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87913805G>A , CM000669.2:g.87913805G>A	GRCh38
NC_000007.13:g.87543120G>A , CM000669.1:g.87543120G>A	GRCh37
NC_000007.12:g.87381056G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927723.1:n.148+96C>T
XR_927724.1:n.192+96C>T