Canonical Allele Identifier: CA691969168
Gene:

Linked Data

dbSNP Id: rs1014365957
MyVariant Identifiers: chr12:g.76398760G>T (hg19) chr12:g.76004980G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004980G>T , CM000674.2:g.76004980G>T GRCh38
NC_000012.11:g.76398760G>T , CM000674.1:g.76398760G>T GRCh37
NC_000012.10:g.74685027G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945110.1:n.311+1209C>A
XR_001749218.2:n.402+1209C>A
XR_945110.3:n.402+1209C>A
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