Canonical Allele Identifier: CA797777129
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1283756959
MyVariant Identifiers: chr4:g.69512318del (hg19) chr4:g.68646600del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646601del , CM000666.2:g.68646601del GRCh38
NC_000004.11:g.69512319del , CM000666.1:g.69512319del GRCh37
NC_000004.10:g.69194914del NCBI36
NG_052676.1:g.29177del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*504del MANE Select ENSP00000341045.5:n.*504del
ENST00000616841.4:c.1732+365del ENSP00000482004.1:n.1732+365del
NM_001076.3:c.*504del NP_001067.2:n.*504del
NM_001076.4:c.*504del MANE Select NP_001067.2:n.*504del
Search 100 bp 5'
Search 100 bp 3'