Canonical Allele Identifier: CA513685590

Gene:

Linked Data

• gnomAD v4: 22-23573072-C-T
• MyVariant Identifiers: chr22:g.23915259C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573072C>T , CM000684.2:g.23573072C>T	GRCh38
NC_000022.10:g.23915259C>T , CM000684.1:g.23915259C>T	GRCh37
NC_000022.9:g.22245259C>T	NCBI36
NG_009791.1:g.12237G>A , LRG_69:g.12237G>A

Transcript Alleles

HGVS	Amino-acid Change
XR_938075.1:n.713C>T
XR_938076.1:n.778C>T
XR_938078.1:n.677C>T
XR_938079.1:n.570C>T
XR_938075.2:n.1297C>T
XR_938078.2:n.1261C>T