Canonical Allele Identifier: CA2670844519

Gene: UGT2B15

Linked Data

• gnomAD v4: 4-68669792-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68669795del , CM000666.2:g.68669795del	GRCh38
NC_000004.11:g.69535513del , CM000666.1:g.69535513del	GRCh37
NC_000004.10:g.69218108del	NCBI36
NG_052676.1:g.5984del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.724+102del MANE Select	ENSP00000341045.5:n.724+102del
ENST00000338206.5:c.724+102del	ENSP00000341045.5:n.724+102del
ENST00000616841.4:c.724+102del	ENSP00000482004.1:n.724+102del
NM_001076.3:c.724+102del	NP_001067.2:n.724+102del
NM_001076.4:c.724+102del MANE Select	NP_001067.2:n.724+102del