Canonical Allele Identifier: CA2016467077
Gene: PRB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11495484C= , CM000674.2:g.11495484C= GRCh38
NC_000012.11:g.11648418C= , CM000674.1:g.11648418C= GRCh37
NC_000012.10:g.11539685C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000545829.1:n.364+5194G=