Canonical Allele Identifier: CA513685622

Gene:

Linked Data

• gnomAD v4: 22-23573083-T-C
• MyVariant Identifiers: chr22:g.23915270T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573083T>C , CM000684.2:g.23573083T>C	GRCh38
NC_000022.10:g.23915270T>C , CM000684.1:g.23915270T>C	GRCh37
NC_000022.9:g.22245270T>C	NCBI36
NG_009791.1:g.12226A>G , LRG_69:g.12226A>G

Transcript Alleles

HGVS	Amino-acid Change
XR_938078.1:n.688T>C
XR_938078.2:n.1272T>C