Canonical Allele Identifier: CA513685639
Gene:

Linked Data

gnomAD v4: 22-23573089-T-G
MyVariant Identifiers: chr22:g.23915276T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573089T>G , CM000684.2:g.23573089T>G GRCh38
NC_000022.10:g.23915276T>G , CM000684.1:g.23915276T>G GRCh37
NC_000022.9:g.22245276T>G NCBI36
NG_009791.1:g.12220A>C , LRG_69:g.12220A>C

Transcript Alleles

HGVS Amino-acid Change
XR_938078.1:n.694T>G
XR_938078.2:n.1278T>G
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