Canonical Allele Identifier: CA2580914745
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.9011169C>A , CM000672.2:g.9011169C>A GRCh38
NC_000010.10:g.9053132C>A , CM000672.1:g.9053132C>A GRCh37
NC_000010.9:g.9093138C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.32+54194G>T