Canonical Allele Identifier: CA513685585
Gene:

Linked Data

gnomAD v4: 22-23573071-C-A
MyVariant Identifiers: chr22:g.23915258C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573071C>A , CM000684.2:g.23573071C>A GRCh38
NC_000022.10:g.23915258C>A , CM000684.1:g.23915258C>A GRCh37
NC_000022.9:g.22245258C>A NCBI36
NG_009791.1:g.12238G>T , LRG_69:g.12238G>T

Transcript Alleles

HGVS Amino-acid Change
XR_938075.1:n.712C>A
XR_938076.1:n.777C>A
XR_938078.1:n.676C>A
XR_938079.1:n.569C>A
XR_938075.2:n.1296C>A
XR_938078.2:n.1260C>A
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