Canonical Allele Identifier: CA552177728

Gene: UGT2B15

Linked Data

• gnomAD v2: 4-69512363-TGGATGACACTTTA-T
• MyVariant Identifiers: chr4:g.69512364_69512376del (hg19) ; chr4:g.68646646_68646658del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646646_68646658del , CM000666.2:g.68646646_68646658del	GRCh38
NC_000004.11:g.69512364_69512376del , CM000666.1:g.69512364_69512376del	GRCh37
NC_000004.10:g.69194959_69194971del	NCBI36
NG_052676.1:g.29119_29131del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*446_*458del MANE Select	ENSP00000341045.5:n.*446_*458del
ENST00000338206.5:c.*446_*458del	ENSP00000341045.5:n.*446_*458del
ENST00000616841.4:c.1732+307_1732+319del	ENSP00000482004.1:n.1732+307_1732+319del
NM_001076.3:c.*446_*458del	NP_001067.2:n.*446_*458del
NM_001076.4:c.*446_*458del MANE Select	NP_001067.2:n.*446_*458del