Canonical Allele Identifier: CA797777356
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1430063842
gnomAD v3: 4-68646743-CT-C
gnomAD v4: 4-68646743-CT-C
MyVariant Identifiers: chr4:g.69512462del (hg19) chr4:g.68646744del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646750del , CM000666.2:g.68646750del GRCh38
NC_000004.11:g.69512468del , CM000666.1:g.69512468del GRCh37
NC_000004.10:g.69195063del NCBI36
NG_052676.1:g.29033del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*360del MANE Select ENSP00000341045.5:n.*360del
ENST00000338206.5:c.*360del ENSP00000341045.5:n.*360del
ENST00000616841.4:c.1732+221del ENSP00000482004.1:n.1732+221del
NM_001076.3:c.*360del NP_001067.2:n.*360del
NM_001076.4:c.*360del MANE Select NP_001067.2:n.*360del
Search 100 bp 5'
Search 100 bp 3'