Canonical Allele Identifier: CA2670844606
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670701-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670701A>C , CM000666.2:g.68670701A>C GRCh38
NC_000004.11:g.69536419A>C , CM000666.1:g.69536419A>C GRCh37
NC_000004.10:g.69219014A>C NCBI36
NG_052676.1:g.5076T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-83T>G NP_001067.2:n.-83T>G