Canonical Allele Identifier: CA1465820678
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1732475138
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646607T>C , CM000666.2:g.68646607T>C GRCh38
NC_000004.11:g.69512325T>C , CM000666.1:g.69512325T>C GRCh37
NC_000004.10:g.69194920T>C NCBI36
NG_052676.1:g.29170A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*497A>G MANE Select ENSP00000341045.5:n.*497A>G
ENST00000616841.4:c.1732+358A>G ENSP00000482004.1:n.1732+358A>G
NM_001076.3:c.*497A>G NP_001067.2:n.*497A>G
NM_001076.4:c.*497A>G MANE Select NP_001067.2:n.*497A>G
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