Canonical Allele Identifier: CA2670844512
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs2109838085
gnomAD v4: 4-68669779-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669779G>A , CM000666.2:g.68669779G>A GRCh38
NC_000004.11:g.69535497G>A , CM000666.1:g.69535497G>A GRCh37
NC_000004.10:g.69218092G>A NCBI36
NG_052676.1:g.5998C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+116C>T MANE Select ENSP00000341045.5:n.724+116C>T
ENST00000338206.5:c.724+116C>T ENSP00000341045.5:n.724+116C>T
ENST00000616841.4:c.724+116C>T ENSP00000482004.1:n.724+116C>T
NM_001076.3:c.724+116C>T NP_001067.2:n.724+116C>T
NM_001076.4:c.724+116C>T MANE Select NP_001067.2:n.724+116C>T
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