Canonical Allele Identifier: CA2670843648
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68646942-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646942G>T , CM000666.2:g.68646942G>T GRCh38
NC_000004.11:g.69512660G>T , CM000666.1:g.69512660G>T GRCh37
NC_000004.10:g.69195255G>T NCBI36
NG_052676.1:g.28835C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*162C>A MANE Select ENSP00000341045.5:n.*162C>A
ENST00000338206.5:c.*162C>A ENSP00000341045.5:n.*162C>A
ENST00000616841.4:c.1732+23C>A ENSP00000482004.1:n.1732+23C>A
NM_001076.3:c.*162C>A NP_001067.2:n.*162C>A
NM_001076.4:c.*162C>A MANE Select NP_001067.2:n.*162C>A