Canonical Allele Identifier: CA619976112
Gene:

Linked Data

dbSNP Id: rs962515543

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782421G>A , CM000677.2:g.95782421G>A GRCh38
NC_000015.9:g.96325650G>A , CM000677.1:g.96325650G>A GRCh37
NC_000015.8:g.94126654G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932654.1:n.148-42768G>A