Canonical Allele Identifier: CA575244622

Gene:

Linked Data

• dbSNP Id: rs1266528530
• gnomAD v2: 7-68611948-T-A
• gnomAD v3: 7-69146961-T-A
• gnomAD v4: 7-69146961-T-A
• MyVariant Identifiers: chr7:g.68611948T>A (hg19) ; chr7:g.69146961T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.69146961T>A , CM000669.2:g.69146961T>A	GRCh38
NC_000007.13:g.68611948T>A , CM000669.1:g.68611948T>A	GRCh37
NC_000007.12:g.68249884T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927647.1:n.88-835A>T