Canonical Allele Identifier: CA2670843356
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68646590-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646590A>G , CM000666.2:g.68646590A>G GRCh38
NC_000004.11:g.69512308A>G , CM000666.1:g.69512308A>G GRCh37
NC_000004.10:g.69194903A>G NCBI36
NG_052676.1:g.29187T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000616841.4:c.1732+375T>C ENSP00000482004.1:n.1732+375T>C