Canonical Allele Identifier: CA2670843683
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68646974-TCTTAACAAGGTAAGTTGTGAAAAGATGTTTTGTCACAGGAAAAAGGAAATCCTCCATTTAAAACCCTCCATGC-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646975_68647047del , CM000666.2:g.68646975_68647047del GRCh38
NC_000004.11:g.69512693_69512765del , CM000666.1:g.69512693_69512765del GRCh37
NC_000004.10:g.69195288_69195360del NCBI36
NG_052676.1:g.28730_28802del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*57_*129del MANE Select ENSP00000341045.5:n.*57_*129del
ENST00000338206.5:c.*57_*129del ENSP00000341045.5:n.*57_*129del
ENST00000616841.4:c.1650_1722del ENSP00000482004.1:n.1650_1722del
NM_001076.3:c.*57_*129del NP_001067.2:n.*57_*129del
NM_001076.4:c.*57_*129del MANE Select NP_001067.2:n.*57_*129del
Search 100 bp 5'
Search 100 bp 3'