Canonical Allele Identifier: CA1898741253
Gene:

Linked Data

dbSNP Id: rs151001092

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075698C>A , CM000672.2:g.29075698C>A GRCh38
NC_000010.10:g.29364627C>A , CM000672.1:g.29364627C>A GRCh37
NC_000010.9:g.29404633C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001747284.1:n.127-3794C>A