Canonical Allele Identifier: CA1465820669
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1732474594
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646597T>A , CM000666.2:g.68646597T>A GRCh38
NC_000004.11:g.69512315T>A , CM000666.1:g.69512315T>A GRCh37
NC_000004.10:g.69194910T>A NCBI36
NG_052676.1:g.29180A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*507A>T MANE Select ENSP00000341045.5:n.*507A>T
ENST00000616841.4:c.1732+368A>T ENSP00000482004.1:n.1732+368A>T
NM_001076.3:c.*507A>T NP_001067.2:n.*507A>T
NM_001076.4:c.*507A>T MANE Select NP_001067.2:n.*507A>T
Search 100 bp 5'
Search 100 bp 3'