Canonical Allele Identifier: CA797777947
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1276696482
MyVariant Identifiers: chr4:g.69512923del (hg19) chr4:g.68647205del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647206del , CM000666.2:g.68647206del GRCh38
NC_000004.11:g.69512924del , CM000666.1:g.69512924del GRCh37
NC_000004.10:g.69195519del NCBI36
NG_052676.1:g.28572del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1492del MANE Select ENSP00000341045.5:p.Leu498CysfsTer8
ENST00000338206.5:c.1492del ENSP00000341045.5:p.Leu498CysfsTer8
ENST00000616841.4:c.1492del ENSP00000482004.1:p.Leu498CysfsTer8
NM_001076.3:c.1492del NP_001067.2:p.Leu498CysfsTer8
NM_001076.4:c.1492del MANE Select NP_001067.2:p.Leu498CysfsTer8
Search 100 bp 5'
Search 100 bp 3'