Canonical Allele Identifier: CA797777656
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1197387928
gnomAD v3: 4-68647013-G-GA
gnomAD v4: 4-68647013-G-GA
MyVariant Identifiers: chr4:g.69512731_69512732insA (hg19) chr4:g.68647013_68647014insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647018dup , CM000666.2:g.68647018dup GRCh38
NC_000004.11:g.69512736dup , CM000666.1:g.69512736dup GRCh37
NC_000004.10:g.69195331dup NCBI36
NG_052676.1:g.28763dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*90dup MANE Select ENSP00000341045.5:n.*90dup
ENST00000338206.5:c.*90dup ENSP00000341045.5:n.*90dup
ENST00000616841.4:c.1683dup ENSP00000482004.1:n.1683dup
NM_001076.3:c.*90dup NP_001067.2:n.*90dup
NM_001076.4:c.*90dup MANE Select NP_001067.2:n.*90dup
Search 100 bp 5'
Search 100 bp 3'