Canonical Allele Identifier: CA1465820657
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646587T= , CM000666.2:g.68646587T= GRCh38
NC_000004.11:g.69512305T= , CM000666.1:g.69512305T= GRCh37
NC_000004.10:g.69194900T= NCBI36
NG_052676.1:g.29190A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000616841.4:c.1732+378A= ENSP00000482004.1:n.1732+378A=