Canonical Allele Identifier: CA2595520106
Gene:

Linked Data

dbSNP Id: rs2140371236

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.69755846G>A , CM000677.2:g.69755846G>A GRCh38
NC_000015.9:g.70048185G>A , CM000677.1:g.70048185G>A GRCh37
NC_000015.8:g.67835239G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001751592.2:n.86-310G>A