Canonical Allele Identifier: CA2670844639
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670767-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670767C>A , CM000666.2:g.68670767C>A GRCh38
NC_000004.11:g.69536485C>A , CM000666.1:g.69536485C>A GRCh37
NC_000004.10:g.69219080C>A NCBI36
NG_052676.1:g.5010G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001076.3:c.-149G>T NP_001067.2:n.-149G>T
Search 100 bp 5'
Search 100 bp 3'