Canonical Allele Identifier: CA989591465
Gene:

Linked Data

dbSNP Id: rs1910117986

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477641T>A , CM000680.2:g.41477641T>A GRCh38
NC_000018.9:g.39057605T>A , CM000680.1:g.39057605T>A GRCh37
NC_000018.8:g.37311603T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935409.1:n.86-26493T>A