Canonical Allele Identifier: CA265579781
Gene:

Linked Data

dbSNP Id: rs577235612

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307327G>A , CM000676.2:g.92307327G>A GRCh38
NC_000014.8:g.92773671G>A , CM000676.1:g.92773671G>A GRCh37
NC_000014.7:g.91843424G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2783G>A