Canonical Allele Identifier: CA439935377
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670295-T-A
MyVariant Identifiers: chr4:g.69536013T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670295T>A , CM000666.2:g.68670295T>A GRCh38
NC_000004.11:g.69536013T>A , CM000666.1:g.69536013T>A GRCh37
NC_000004.10:g.69218608T>A NCBI36
NG_052676.1:g.5482A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.324A>T MANE Select ENSP00000341045.5:p.Ser108=
ENST00000338206.5:c.324A>T ENSP00000341045.5:p.Ser108=
ENST00000616841.4:c.324A>T ENSP00000482004.1:p.Ser108=
NM_001076.3:c.324A>T NP_001067.2:p.Ser108=
NM_001076.4:c.324A>T MANE Select NP_001067.2:p.Ser108=