Canonical Allele Identifier: CA2578102351
Gene: UGT2B15 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669888G>T , CM000666.2:g.68669888G>T GRCh38
NC_000004.11:g.69535606G>T , CM000666.1:g.69535606G>T GRCh37
NC_000004.10:g.69218201G>T NCBI36
NG_052676.1:g.5889C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+7C>A MANE Select ENSP00000341045.5:n.724+7C>A
ENST00000338206.5:c.724+7C>A ENSP00000341045.5:n.724+7C>A
ENST00000616841.4:c.724+7C>A ENSP00000482004.1:n.724+7C>A
NM_001076.3:c.724+7C>A NP_001067.2:n.724+7C>A
NM_001076.4:c.724+7C>A MANE Select NP_001067.2:n.724+7C>A
Search 100 bp 5'
Search 100 bp 3'