Canonical Allele Identifier: CA1465820666
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646596A= , CM000666.2:g.68646596A= GRCh38
NC_000004.11:g.69512314A= , CM000666.1:g.69512314A= GRCh37
NC_000004.10:g.69194909A= NCBI36
NG_052676.1:g.29181T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000616841.4:c.1732+369T= ENSP00000482004.1:n.1732+369T=