Canonical Allele Identifier: CA844313436

Gene:

Linked Data

• dbSNP Id: rs1408340824
• gnomAD v3: 7-97388502-C-T
• gnomAD v4: 7-97388502-C-T
• MyVariant Identifiers: chr7:g.97017814C>T (hg19) ; chr7:g.97388502C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97388502C>T , CM000669.2:g.97388502C>T	GRCh38
NC_000007.13:g.97017814C>T , CM000669.1:g.97017814C>T	GRCh37
NC_000007.12:g.96855750C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001745293.1:n.127-59855G>A