Canonical Allele Identifier: CA513685576
Gene:

Linked Data

MyVariant Identifiers: chr22:g.23915255A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573068A>C , CM000684.2:g.23573068A>C GRCh38
NC_000022.10:g.23915255A>C , CM000684.1:g.23915255A>C GRCh37
NC_000022.9:g.22245255A>C NCBI36
NG_009791.1:g.12241T>G , LRG_69:g.12241T>G

Transcript Alleles

HGVS Amino-acid Change
XR_938075.1:n.709A>C
XR_938076.1:n.774A>C
XR_938078.1:n.673A>C
XR_938079.1:n.566A>C
XR_938075.2:n.1293A>C
XR_938078.2:n.1257A>C
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