Canonical Allele Identifier: CA513685591

Gene:

Linked Data

• gnomAD v4: 22-23573073-A-T
• MyVariant Identifiers: chr22:g.23915260A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573073A>T , CM000684.2:g.23573073A>T	GRCh38
NC_000022.10:g.23915260A>T , CM000684.1:g.23915260A>T	GRCh37
NC_000022.9:g.22245260A>T	NCBI36
NG_009791.1:g.12236T>A , LRG_69:g.12236T>A

Transcript Alleles

HGVS	Amino-acid Change
XR_938075.1:n.714A>T
XR_938076.1:n.779A>T
XR_938078.1:n.678A>T
XR_938079.1:n.571A>T
XR_938075.2:n.1298A>T
XR_938078.2:n.1262A>T