Canonical Allele Identifier: CA1465821025
Gene: UGT2B15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647168_68647169delinsGT , CM000666.2:g.68647168_68647169delinsGT GRCh38
NC_000004.11:g.69512886_69512887delinsGT , CM000666.1:g.69512886_69512887delinsGT GRCh37
NC_000004.10:g.69195481_69195482delinsGT NCBI36
NG_052676.1:g.28608_28609delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1528_1529delinsAC MANE Select ENSP00000341045.5:p.Thr510=
ENST00000338206.5:c.1528_1529delinsAC ENSP00000341045.5:p.Thr510=
ENST00000616841.4:c.1528_1529delinsAC ENSP00000482004.1:p.Thr510=
NM_001076.3:c.1528_1529delinsAC NP_001067.2:p.Thr510=
NM_001076.4:c.1528_1529delinsAC MANE Select NP_001067.2:p.Thr510=
Search 100 bp 5'
Search 100 bp 3'