Canonical Allele Identifier: CA2670843592

Gene: UGT2B15

Linked Data

• gnomAD v4: 4-68646909-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646914del , CM000666.2:g.68646914del	GRCh38
NC_000004.11:g.69512632del , CM000666.1:g.69512632del	GRCh37
NC_000004.10:g.69195227del	NCBI36
NG_052676.1:g.28867del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*194del MANE Select	ENSP00000341045.5:n.*194del
ENST00000338206.5:c.*194del	ENSP00000341045.5:n.*194del
ENST00000616841.4:c.1732+55del	ENSP00000482004.1:n.1732+55del
NM_001076.3:c.*194del	NP_001067.2:n.*194del
NM_001076.4:c.*194del MANE Select	NP_001067.2:n.*194del