Canonical Allele Identifier: CA1104780622

Gene:

Linked Data

• gnomAD v3: 7-97388465-A-T
• gnomAD v4: 7-97388465-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.97388465A>T , CM000669.2:g.97388465A>T	GRCh38
NC_000007.13:g.97017777A>T , CM000669.1:g.97017777A>T	GRCh37
NC_000007.12:g.96855713A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001745293.1:n.127-59818T>A