Canonical Allele Identifier: CA322555667

Gene:

Linked Data

• dbSNP Id: rs112411922
• gnomAD v3: 22-23573075-G-A
• gnomAD v4: 22-23573075-G-A
• MyVariant Identifiers: chr22:g.23915262G>A (hg19) ; chr22:g.23573075G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573075G>A , CM000684.2:g.23573075G>A	GRCh38
NC_000022.10:g.23915262G>A , CM000684.1:g.23915262G>A	GRCh37
NC_000022.9:g.22245262G>A	NCBI36
NG_009791.1:g.12234C>T , LRG_69:g.12234C>T

Transcript Alleles

HGVS	Amino-acid Change
XR_938078.1:n.680G>A
XR_938078.2:n.1264G>A