Canonical Allele Identifier: CA797795839
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1254363027
gnomAD v3: 4-68670757-A-T
gnomAD v4: 4-68670757-A-T
MyVariant Identifiers: chr4:g.69536475A>T (hg19) chr4:g.68670757A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670757A>T , CM000666.2:g.68670757A>T GRCh38
NC_000004.11:g.69536475A>T , CM000666.1:g.69536475A>T GRCh37
NC_000004.10:g.69219070A>T NCBI36
NG_052676.1:g.5020T>A

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-139T>A NP_001067.2:n.-139T>A
Search 100 bp 5'
Search 100 bp 3'