Canonical Allele Identifier: CA973101870
Gene:

Linked Data

dbSNP Id: rs1899530207

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782350G>A , CM000677.2:g.95782350G>A GRCh38
NC_000015.9:g.96325579G>A , CM000677.1:g.96325579G>A GRCh37
NC_000015.8:g.94126583G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932654.1:n.148-42839G>A