Canonical Allele Identifier: CA1465820676
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1222289636
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646606A>T , CM000666.2:g.68646606A>T GRCh38
NC_000004.11:g.69512324A>T , CM000666.1:g.69512324A>T GRCh37
NC_000004.10:g.69194919A>T NCBI36
NG_052676.1:g.29171T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*498T>A MANE Select ENSP00000341045.5:n.*498T>A
ENST00000616841.4:c.1732+359T>A ENSP00000482004.1:n.1732+359T>A
NM_001076.3:c.*498T>A NP_001067.2:n.*498T>A
NM_001076.4:c.*498T>A MANE Select NP_001067.2:n.*498T>A
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