Canonical Allele Identifier: CA2578102340

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68669801A>G , CM000666.2:g.68669801A>G	GRCh38
NC_000004.11:g.69535519A>G , CM000666.1:g.69535519A>G	GRCh37
NC_000004.10:g.69218114A>G	NCBI36
NG_052676.1:g.5976T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.724+94T>C MANE Select	ENSP00000341045.5:n.724+94T>C
ENST00000338206.5:c.724+94T>C	ENSP00000341045.5:n.724+94T>C
ENST00000616841.4:c.724+94T>C	ENSP00000482004.1:n.724+94T>C
NM_001076.3:c.724+94T>C	NP_001067.2:n.724+94T>C
NM_001076.4:c.724+94T>C MANE Select	NP_001067.2:n.724+94T>C