Canonical Allele Identifier: CA2762060776
Gene: UGT2B15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647134_68647136del , CM000666.2:g.68647134_68647136del GRCh38
NC_000004.11:g.69512852_69512854del , CM000666.1:g.69512852_69512854del GRCh37
NC_000004.10:g.69195447_69195449del NCBI36
NG_052676.1:g.28641_28643del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1561_1563del MANE Select ENSP00000341045.5:p.Ala521del
ENST00000338206.5:c.1561_1563del ENSP00000341045.5:p.Ala521del
ENST00000616841.4:c.1561_1563del ENSP00000482004.1:p.Ala521del
NM_001076.3:c.1561_1563del NP_001067.2:p.Ala521del
NM_001076.4:c.1561_1563del MANE Select NP_001067.2:p.Ala521del
Search 100 bp 5'
Search 100 bp 3'