Canonical Allele Identifier: CA797777592

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1195246559
• MyVariant Identifiers: chr4:g.69512655_69512656insCAA (hg19) ; chr4:g.68646937_68646938insCAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646937_68646938insCAA , CM000666.2:g.68646937_68646938insCAA	GRCh38
NC_000004.11:g.69512655_69512656insCAA , CM000666.1:g.69512655_69512656insCAA	GRCh37
NC_000004.10:g.69195250_69195251insCAA	NCBI36
NG_052676.1:g.28839_28840insTTG

Transcript Alleles

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