Canonical Allele Identifier: CA858671720
Gene:

Linked Data

dbSNP Id: rs1258843888
MyVariant Identifiers: chr9:g.113998991G>A (hg19) chr9:g.111236711G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.111236711G>A , CM000671.2:g.111236711G>A GRCh38
NC_000009.11:g.113998991G>A , CM000671.1:g.113998991G>A GRCh37
NC_000009.10:g.113038812G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930247.1:n.476+36102C>T
XR_930248.1:n.556+36102C>T
XR_930249.1:n.476+36102C>T
XR_001746893.1:n.476+36102C>T
XR_001746894.1:n.476+36102C>T
XR_930247.2:n.476+36102C>T
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