Canonical Allele Identifier: CA844313405

Gene:

Linked Data

• dbSNP Id: rs1331052520
• MyVariant Identifiers: chr7:g.97017669G>A (hg19) ; chr7:g.97388357G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97388357G>A , CM000669.2:g.97388357G>A	GRCh38
NC_000007.13:g.97017669G>A , CM000669.1:g.97017669G>A	GRCh37
NC_000007.12:g.96855605G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001745293.1:n.127-59710C>T