Canonical Allele Identifier: CA2670844641
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670771-G-C

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-153C>G NP_001067.2:n.-153C>G