Canonical Allele Identifier: CA552612245
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1258969746
gnomAD v2: 4-69535580-A-G
gnomAD v4: 4-68669862-A-G
MyVariant Identifiers: chr4:g.69535580A>G (hg19) chr4:g.68669862A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669862A>G , CM000666.2:g.68669862A>G GRCh38
NC_000004.11:g.69535580A>G , CM000666.1:g.69535580A>G GRCh37
NC_000004.10:g.69218175A>G NCBI36
NG_052676.1:g.5915T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+33T>C MANE Select ENSP00000341045.5:n.724+33T>C
ENST00000338206.5:c.724+33T>C ENSP00000341045.5:n.724+33T>C
ENST00000616841.4:c.724+33T>C ENSP00000482004.1:n.724+33T>C
NM_001076.3:c.724+33T>C NP_001067.2:n.724+33T>C
NM_001076.4:c.724+33T>C MANE Select NP_001067.2:n.724+33T>C
Search 100 bp 5'
Search 100 bp 3'