Canonical Allele Identifier: CA685452810
Gene:

Linked Data

dbSNP Id: rs1215966934
MyVariant Identifiers: chr12:g.132014149G>T (hg19) chr12:g.131529604G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529604G>T , CM000674.2:g.131529604G>T GRCh38
NC_000012.11:g.132014149G>T , CM000674.1:g.132014149G>T GRCh37
NC_000012.10:g.130580102G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+171C>A
XR_001749407.2:n.1067+171C>A
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