Canonical Allele Identifier: CA1465820660
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646592G= , CM000666.2:g.68646592G= GRCh38
NC_000004.11:g.69512310G= , CM000666.1:g.69512310G= GRCh37
NC_000004.10:g.69194905G= NCBI36
NG_052676.1:g.29185C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000616841.4:c.1732+373C= ENSP00000482004.1:n.1732+373C=