Canonical Allele Identifier: CA2670844530
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68669818-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669818T>C , CM000666.2:g.68669818T>C GRCh38
NC_000004.11:g.69535536T>C , CM000666.1:g.69535536T>C GRCh37
NC_000004.10:g.69218131T>C NCBI36
NG_052676.1:g.5959A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+77A>G MANE Select ENSP00000341045.5:n.724+77A>G
ENST00000338206.5:c.724+77A>G ENSP00000341045.5:n.724+77A>G
ENST00000616841.4:c.724+77A>G ENSP00000482004.1:n.724+77A>G
NM_001076.3:c.724+77A>G NP_001067.2:n.724+77A>G
NM_001076.4:c.724+77A>G MANE Select NP_001067.2:n.724+77A>G
Search 100 bp 5'
Search 100 bp 3'