Canonical Allele Identifier: CA2670843660
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68646950-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646950T>A , CM000666.2:g.68646950T>A GRCh38
NC_000004.11:g.69512668T>A , CM000666.1:g.69512668T>A GRCh37
NC_000004.10:g.69195263T>A NCBI36
NG_052676.1:g.28827A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*154A>T MANE Select ENSP00000341045.5:n.*154A>T
ENST00000338206.5:c.*154A>T ENSP00000341045.5:n.*154A>T
ENST00000616841.4:c.1732+15A>T ENSP00000482004.1:n.1732+15A>T
NM_001076.3:c.*154A>T NP_001067.2:n.*154A>T
NM_001076.4:c.*154A>T MANE Select NP_001067.2:n.*154A>T