Canonical Allele Identifier: CA160479201

Gene:

Linked Data

• dbSNP Id: rs932347159
• gnomAD v3: 7-69146907-G-T
• gnomAD v4: 7-69146907-G-T
• MyVariant Identifiers: chr7:g.68611894G>T (hg19) ; chr7:g.69146907G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.69146907G>T , CM000669.2:g.69146907G>T	GRCh38
NC_000007.13:g.68611894G>T , CM000669.1:g.68611894G>T	GRCh37
NC_000007.12:g.68249830G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_927647.1:n.88-781C>A