Canonical Allele Identifier: CA1063770057

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1733244931
• gnomAD v3: 4-68669768-A-G
• gnomAD v4: 4-68669768-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68669768A>G , CM000666.2:g.68669768A>G	GRCh38
NC_000004.11:g.69535486A>G , CM000666.1:g.69535486A>G	GRCh37
NC_000004.10:g.69218081A>G	NCBI36
NG_052676.1:g.6009T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.724+127T>C MANE Select	ENSP00000341045.5:n.724+127T>C
ENST00000338206.5:c.724+127T>C	ENSP00000341045.5:n.724+127T>C
ENST00000616841.4:c.724+127T>C	ENSP00000482004.1:n.724+127T>C
NM_001076.3:c.724+127T>C	NP_001067.2:n.724+127T>C
NM_001076.4:c.724+127T>C MANE Select	NP_001067.2:n.724+127T>C