Canonical Allele Identifier: CA1063752842
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1732491723
gnomAD v3: 4-68646954-TC-T
gnomAD v4: 4-68646954-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646957del , CM000666.2:g.68646957del GRCh38
NC_000004.11:g.69512675del , CM000666.1:g.69512675del GRCh37
NC_000004.10:g.69195270del NCBI36
NG_052676.1:g.28822del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*149del MANE Select ENSP00000341045.5:n.*149del
ENST00000338206.5:c.*149del ENSP00000341045.5:n.*149del
ENST00000616841.4:c.1732+10del ENSP00000482004.1:n.1732+10del
NM_001076.3:c.*149del NP_001067.2:n.*149del
NM_001076.4:c.*149del MANE Select NP_001067.2:n.*149del
Search 100 bp 5'
Search 100 bp 3'