Canonical Allele Identifier: CA513685656

Gene:

Linked Data

• gnomAD v4: 22-23573095-A-G
• MyVariant Identifiers: chr22:g.23915282A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573095A>G , CM000684.2:g.23573095A>G	GRCh38
NC_000022.10:g.23915282A>G , CM000684.1:g.23915282A>G	GRCh37
NC_000022.9:g.22245282A>G	NCBI36
NG_009791.1:g.12214T>C , LRG_69:g.12214T>C

Transcript Alleles

HGVS	Amino-acid Change
XR_938078.1:n.700A>G
XR_938078.2:n.1284A>G