Canonical Allele Identifier: CA2670843640

Gene: UGT2B15

Linked Data

• gnomAD v4: 4-68646937-C-CAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646937_68646938insAAA , CM000666.2:g.68646937_68646938insAAA	GRCh38
NC_000004.11:g.69512655_69512656insAAA , CM000666.1:g.69512655_69512656insAAA	GRCh37
NC_000004.10:g.69195250_69195251insAAA	NCBI36
NG_052676.1:g.28839_28840insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*166_*167insTTT MANE Select	ENSP00000341045.5:n.*166_*167insTTT
ENST00000338206.5:c.*166_*167insTTT	ENSP00000341045.5:n.*166_*167insTTT
ENST00000616841.4:c.1732+27_1732+28insTTT	ENSP00000482004.1:n.1732+27_1732+28insTTT
NM_001076.3:c.*166_*167insTTT	NP_001067.2:n.*166_*167insTTT
NM_001076.4:c.*166_*167insTTT MANE Select	NP_001067.2:n.*166_*167insTTT