Canonical Allele Identifier: CA513685562

Gene:

Linked Data

• gnomAD v4: 22-23573064-T-C
• MyVariant Identifiers: chr22:g.23915251T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23573064T>C , CM000684.2:g.23573064T>C	GRCh38
NC_000022.10:g.23915251T>C , CM000684.1:g.23915251T>C	GRCh37
NC_000022.9:g.22245251T>C	NCBI36
NG_009791.1:g.12245A>G , LRG_69:g.12245A>G

Transcript Alleles

HGVS	Amino-acid Change
XR_938075.1:n.705T>C
XR_938076.1:n.770T>C
XR_938078.1:n.669T>C
XR_938079.1:n.562T>C
XR_938075.2:n.1289T>C
XR_938078.2:n.1253T>C