Canonical Allele Identifier: CA2670844589
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670665-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670665C>T , CM000666.2:g.68670665C>T GRCh38
NC_000004.11:g.69536383C>T , CM000666.1:g.69536383C>T GRCh37
NC_000004.10:g.69218978C>T NCBI36
NG_052676.1:g.5112G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-47G>A NP_001067.2:n.-47G>A