Canonical Allele Identifier: CA287548520
Gene:

Linked Data

dbSNP Id: rs902509729
MyVariant Identifiers: chr17:g.8040762G>A (hg19) chr17:g.8137444G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137444G>A , CM000679.2:g.8137444G>A GRCh38
NC_000017.10:g.8040762G>A , CM000679.1:g.8040762G>A GRCh37
NC_000017.9:g.7981487G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1405G>A
XR_934203.1:n.70-2033G>A
XR_934202.2:n.414-1405G>A
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