Canonical Allele Identifier: CA552185664
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1372862338
gnomAD v2: 4-69536358-T-C
MyVariant Identifiers: chr4:g.69536358T>C (hg19) chr4:g.68670640T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670640T>C , CM000666.2:g.68670640T>C GRCh38
NC_000004.11:g.69536358T>C , CM000666.1:g.69536358T>C GRCh37
NC_000004.10:g.69218953T>C NCBI36
NG_052676.1:g.5137A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.-22A>G MANE Select ENSP00000341045.5:n.-22A>G
NM_001076.3:c.-22A>G NP_001067.2:n.-22A>G
NM_001076.4:c.-22A>G MANE Select NP_001067.2:n.-22A>G
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