Canonical Allele Identifier: CA513685566

Gene:

Linked Data

• gnomAD v4: 22-23573065-G-T
• MyVariant Identifiers: chr22:g.23915252G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573065G>T , CM000684.2:g.23573065G>T	GRCh38
NC_000022.10:g.23915252G>T , CM000684.1:g.23915252G>T	GRCh37
NC_000022.9:g.22245252G>T	NCBI36
NG_009791.1:g.12244C>A , LRG_69:g.12244C>A

Transcript Alleles

HGVS	Amino-acid Change
XR_938075.1:n.706G>T
XR_938076.1:n.771G>T
XR_938078.1:n.670G>T
XR_938079.1:n.563G>T
XR_938075.2:n.1290G>T
XR_938078.2:n.1254G>T