Canonical Allele Identifier: CA322555664
Gene:

Linked Data

dbSNP Id: rs186565150
gnomAD v2: 22-23915260-A-G
gnomAD v3: 22-23573073-A-G
gnomAD v4: 22-23573073-A-G
MyVariant Identifiers: chr22:g.23915260A>G (hg19) chr22:g.23573073A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573073A>G , CM000684.2:g.23573073A>G GRCh38
NC_000022.10:g.23915260A>G , CM000684.1:g.23915260A>G GRCh37
NC_000022.9:g.22245260A>G NCBI36
NG_009791.1:g.12236T>C , LRG_69:g.12236T>C

Transcript Alleles

HGVS Amino-acid Change
XR_938075.1:n.714A>G
XR_938076.1:n.779A>G
XR_938078.1:n.678A>G
XR_938079.1:n.571A>G
XR_938075.2:n.1298A>G
XR_938078.2:n.1262A>G
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