Canonical Allele Identifier: CA1465795133
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1560613816
gnomAD v4: 4-68670771-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670771G>A , CM000666.2:g.68670771G>A GRCh38
NC_000004.11:g.69536489G>A , CM000666.1:g.69536489G>A GRCh37
NC_000004.10:g.69219084G>A NCBI36
NG_052676.1:g.5006C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-153C>T NP_001067.2:n.-153C>T
Search 100 bp 5'
Search 100 bp 3'