Canonical Allele Identifier: CA2670844629
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670758-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670758G>T , CM000666.2:g.68670758G>T GRCh38
NC_000004.11:g.69536476G>T , CM000666.1:g.69536476G>T GRCh37
NC_000004.10:g.69219071G>T NCBI36
NG_052676.1:g.5019C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-140C>A NP_001067.2:n.-140C>A
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