Canonical Allele Identifier: CA513685592
Gene:

Linked Data

MyVariant Identifiers: chr22:g.23915260A>C (hg19)
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Genomic Alleles

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

Transcript Alleles

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