Canonical Allele Identifier: CA2670844644
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670773-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670773G>T , CM000666.2:g.68670773G>T GRCh38
NC_000004.11:g.69536491G>T , CM000666.1:g.69536491G>T GRCh37
NC_000004.10:g.69219086G>T NCBI36
NG_052676.1:g.5004C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-155C>A NP_001067.2:n.-155C>A