Canonical Allele Identifier: CA1465793484
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733245038
gnomAD v4: 4-68669770-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669770C>T , CM000666.2:g.68669770C>T GRCh38
NC_000004.11:g.69535488C>T , CM000666.1:g.69535488C>T GRCh37
NC_000004.10:g.69218083C>T NCBI36
NG_052676.1:g.6007G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+125G>A MANE Select ENSP00000341045.5:n.724+125G>A
ENST00000338206.5:c.724+125G>A ENSP00000341045.5:n.724+125G>A
ENST00000616841.4:c.724+125G>A ENSP00000482004.1:n.724+125G>A
NM_001076.3:c.724+125G>A NP_001067.2:n.724+125G>A
NM_001076.4:c.724+125G>A MANE Select NP_001067.2:n.724+125G>A
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