Canonical Allele Identifier: CA1140000321
Gene: EBNA1BP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43255323A= , CM000663.2:g.43255323A= GRCh38
NC_000001.10:g.43720994A= , CM000663.1:g.43720994A= GRCh37
NC_000001.9:g.43493581A= NCBI36
NG_028079.2:g.87994A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461557.2:n.108+6519T=
ENST00000466927.5:n.69+6519T=