Canonical Allele Identifier: CA797777315
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs4148274
gnomAD v3: 4-68646729-A-ATTTTTT
gnomAD v4: 4-68646729-A-ATTTTTT
MyVariant Identifiers: chr4:g.69512447_69512448insTTTTTT (hg19) chr4:g.68646729_68646730insTTTTTT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646736_68646741dup , CM000666.2:g.68646736_68646741dup GRCh38
NC_000004.11:g.69512454_69512459dup , CM000666.1:g.69512454_69512459dup GRCh37
NC_000004.10:g.69195049_69195054dup NCBI36
NG_052676.1:g.29042_29047dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*369_*374dup MANE Select ENSP00000341045.5:n.*369_*374dup
ENST00000338206.5:c.*369_*374dup ENSP00000341045.5:n.*369_*374dup
ENST00000616841.4:c.1732+230_1732+235dup ENSP00000482004.1:n.1732+230_1732+235dup
NM_001076.3:c.*369_*374dup NP_001067.2:n.*369_*374dup
NM_001076.4:c.*369_*374dup MANE Select NP_001067.2:n.*369_*374dup
Search 100 bp 5'
Search 100 bp 3'