Canonical Allele Identifier: CA513685617

Gene:

Linked Data

• gnomAD v4: 22-23573081-C-T
• MyVariant Identifiers: chr22:g.23915268C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573081C>T , CM000684.2:g.23573081C>T	GRCh38
NC_000022.10:g.23915268C>T , CM000684.1:g.23915268C>T	GRCh37
NC_000022.9:g.22245268C>T	NCBI36
NG_009791.1:g.12228G>A , LRG_69:g.12228G>A

Transcript Alleles

HGVS	Amino-acid Change
XR_938078.1:n.686C>T
XR_938078.2:n.1270C>T