Canonical Allele Identifier: CA1465793582
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733248389
gnomAD v4: 4-68669861-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669861A>C , CM000666.2:g.68669861A>C GRCh38
NC_000004.11:g.69535579A>C , CM000666.1:g.69535579A>C GRCh37
NC_000004.10:g.69218174A>C NCBI36
NG_052676.1:g.5916T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+34T>G MANE Select ENSP00000341045.5:n.724+34T>G
ENST00000338206.5:c.724+34T>G ENSP00000341045.5:n.724+34T>G
ENST00000616841.4:c.724+34T>G ENSP00000482004.1:n.724+34T>G
NM_001076.3:c.724+34T>G NP_001067.2:n.724+34T>G
NM_001076.4:c.724+34T>G MANE Select NP_001067.2:n.724+34T>G