Canonical Allele Identifier: CA513685629

Gene:

Linked Data

• gnomAD v4: 22-23573086-C-A
• MyVariant Identifiers: chr22:g.23915273C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573086C>A , CM000684.2:g.23573086C>A	GRCh38
NC_000022.10:g.23915273C>A , CM000684.1:g.23915273C>A	GRCh37
NC_000022.9:g.22245273C>A	NCBI36
NG_009791.1:g.12223G>T , LRG_69:g.12223G>T

Transcript Alleles

HGVS	Amino-acid Change
XR_938078.1:n.691C>A
XR_938078.2:n.1275C>A