Canonical Allele Identifier: CA1465820664
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646593C= , CM000666.2:g.68646593C= GRCh38
NC_000004.11:g.69512311C= , CM000666.1:g.69512311C= GRCh37
NC_000004.10:g.69194906C= NCBI36
NG_052676.1:g.29184G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000616841.4:c.1732+372G= ENSP00000482004.1:n.1732+372G=