Canonical Allele Identifier: CA1465820665
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646595C= , CM000666.2:g.68646595C= GRCh38
NC_000004.11:g.69512313C= , CM000666.1:g.69512313C= GRCh37
NC_000004.10:g.69194908C= NCBI36
NG_052676.1:g.29182G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000616841.4:c.1732+370G= ENSP00000482004.1:n.1732+370G=