Canonical Allele Identifier: CA188145868
Gene:

Linked Data

dbSNP Id: rs1027222535
MyVariant Identifiers: chr9:g.1787569G>A (hg19) chr9:g.1787569G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1787569G>A , CM000671.2:g.1787569G>A GRCh38
NC_000009.11:g.1787569G>A , CM000671.1:g.1787569G>A GRCh37
NC_000009.10:g.1777569G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746599.1:n.142+68657G>A
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