Canonical Allele Identifier: CA692339874
Gene:

Linked Data

dbSNP Id: rs1406542066
MyVariant Identifiers: chr12:g.80462993G>A (hg19) chr12:g.80069213G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80069213G>A , CM000674.2:g.80069213G>A GRCh38
NC_000012.11:g.80462993G>A , CM000674.1:g.80462993G>A GRCh37
NC_000012.10:g.78987124G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945140.1:n.456+8031G>A
XR_945141.1:n.1758+8031G>A
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