Canonical Allele Identifier: CA797777145
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1344093098
gnomAD v3: 4-68646627-TC-T
gnomAD v4: 4-68646627-TC-T
MyVariant Identifiers: chr4:g.69512346del (hg19) chr4:g.68646628del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646628del , CM000666.2:g.68646628del GRCh38
NC_000004.11:g.69512346del , CM000666.1:g.69512346del GRCh37
NC_000004.10:g.69194941del NCBI36
NG_052676.1:g.29149del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*476del MANE Select ENSP00000341045.5:n.*476del
ENST00000616841.4:c.1732+337del ENSP00000482004.1:n.1732+337del
NM_001076.3:c.*476del NP_001067.2:n.*476del
NM_001076.4:c.*476del MANE Select NP_001067.2:n.*476del
Search 100 bp 5'
Search 100 bp 3'