Canonical Allele Identifier: CA693572537
Gene:

Linked Data

dbSNP Id: rs1298732212
MyVariant Identifiers: chr12:g.93686931G>T (hg19) chr12:g.93293155G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93293155G>T , CM000674.2:g.93293155G>T GRCh38
NC_000012.11:g.93686931G>T , CM000674.1:g.93686931G>T GRCh37
NC_000012.10:g.92211062G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040096.1:n.329+34872C>A
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