Canonical Allele Identifier: CA693572600
Gene:

Linked Data

dbSNP Id: rs749273834
MyVariant Identifiers: chr12:g.93687099G>T (hg19) chr12:g.93293323G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293323G>T , CM000674.2:g.93293323G>T GRCh38
NC_000012.11:g.93687099G>T , CM000674.1:g.93687099G>T GRCh37
NC_000012.10:g.92211230G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34704C>A
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