Canonical Allele Identifier: CA663648523
Gene:

Linked Data

dbSNP Id: rs1467444568
MyVariant Identifiers: chr10:g.30490691A>C (hg19) chr10:g.30201762A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201762A>C , CM000672.2:g.30201762A>C GRCh38
NC_000010.10:g.30490691A>C , CM000672.1:g.30490691A>C GRCh37
NC_000010.9:g.30530697A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930791.1:n.1193-1725A>C
XR_930791.2:n.1449-1725A>C
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