Canonical Allele Identifier: CA1465793528

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1434577836

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68669799A>C , CM000666.2:g.68669799A>C	GRCh38
NC_000004.11:g.69535517A>C , CM000666.1:g.69535517A>C	GRCh37
NC_000004.10:g.69218112A>C	NCBI36
NG_052676.1:g.5978T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.724+96T>G MANE Select	ENSP00000341045.5:n.724+96T>G
ENST00000338206.5:c.724+96T>G	ENSP00000341045.5:n.724+96T>G
ENST00000616841.4:c.724+96T>G	ENSP00000482004.1:n.724+96T>G
NM_001076.3:c.724+96T>G	NP_001067.2:n.724+96T>G
NM_001076.4:c.724+96T>G MANE Select	NP_001067.2:n.724+96T>G