Canonical Allele Identifier: CA1063752647
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v3: 4-68646748-T-TTTTAA
gnomAD v4: 4-68646748-T-TTTTAA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646750_68646751insTAATT , CM000666.2:g.68646750_68646751insTAATT GRCh38
NC_000004.11:g.69512468_69512469insTAATT , CM000666.1:g.69512468_69512469insTAATT GRCh37
NC_000004.10:g.69195063_69195064insTAATT NCBI36
NG_052676.1:g.29028_29029insTTAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*355_*356insTTAAA MANE Select ENSP00000341045.5:n.*355_*356insTTAAA
ENST00000338206.5:c.*355_*356insTTAAA ENSP00000341045.5:n.*355_*356insTTAAA
ENST00000616841.4:c.1732+216_1732+217insTTAAA ENSP00000482004.1:n.1732+216_1732+217insTTAAA
NM_001076.3:c.*355_*356insTTAAA NP_001067.2:n.*355_*356insTTAAA
NM_001076.4:c.*355_*356insTTAAA MANE Select NP_001067.2:n.*355_*356insTTAAA
Search 100 bp 5'
Search 100 bp 3'