Canonical Allele Identifier: CA513685579

Gene:

Linked Data

• gnomAD v4: 22-23573069-A-T
• MyVariant Identifiers: chr22:g.23915256A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573069A>T , CM000684.2:g.23573069A>T	GRCh38
NC_000022.10:g.23915256A>T , CM000684.1:g.23915256A>T	GRCh37
NC_000022.9:g.22245256A>T	NCBI36
NG_009791.1:g.12240T>A , LRG_69:g.12240T>A

Transcript Alleles

HGVS	Amino-acid Change
XR_938075.1:n.710A>T
XR_938076.1:n.775A>T
XR_938078.1:n.674A>T
XR_938079.1:n.567A>T
XR_938075.2:n.1294A>T
XR_938078.2:n.1258A>T