Canonical Allele Identifier: CA841571682

Gene:

Linked Data

• dbSNP Id: rs1198985293
• gnomAD v3: 7-69146913-C-T
• gnomAD v4: 7-69146913-C-T
• MyVariant Identifiers: chr7:g.68611900C>T (hg19) ; chr7:g.69146913C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.69146913C>T , CM000669.2:g.69146913C>T	GRCh38
NC_000007.13:g.68611900C>T , CM000669.1:g.68611900C>T	GRCh37
NC_000007.12:g.68249836C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_927647.1:n.88-787G>A