Canonical Allele Identifier: CA513685598
Gene:

Linked Data

MyVariant Identifiers: chr22:g.23915262G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573075G>T , CM000684.2:g.23573075G>T GRCh38
NC_000022.10:g.23915262G>T , CM000684.1:g.23915262G>T GRCh37
NC_000022.9:g.22245262G>T NCBI36
NG_009791.1:g.12234C>A , LRG_69:g.12234C>A

Transcript Alleles

HGVS Amino-acid Change
XR_938078.1:n.680G>T
XR_938078.2:n.1264G>T
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