Canonical Allele Identifier: CA2670843355
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68646588-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646588A>T , CM000666.2:g.68646588A>T GRCh38
NC_000004.11:g.69512306A>T , CM000666.1:g.69512306A>T GRCh37
NC_000004.10:g.69194901A>T NCBI36
NG_052676.1:g.29189T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000616841.4:c.1732+377T>A ENSP00000482004.1:n.1732+377T>A