Canonical Allele Identifier: CA575244617

Gene:

Linked Data

• gnomAD v2: 7-68611909-A-G
• MyVariant Identifiers: chr7:g.68611909A>G (hg19) ; chr7:g.69146922A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.69146922A>G , CM000669.2:g.69146922A>G	GRCh38
NC_000007.13:g.68611909A>G , CM000669.1:g.68611909A>G	GRCh37
NC_000007.12:g.68249845A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_927647.1:n.88-796T>C