Canonical Allele Identifier: CA706619764
Gene:

Linked Data

dbSNP Id: rs1312585158

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50857061G>A , CM000676.2:g.50857061G>A GRCh38
NC_000014.8:g.51323779G>A , CM000676.1:g.51323779G>A GRCh37
NC_000014.7:g.50393529G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1037C>T
XR_943848.2:n.643+1037C>T