Canonical Allele Identifier: CA2942664

Gene: UGT2B15

Linked Data

• dbSNP Id: rs781244499
• ExAC: 4:69535682 G / T
• gnomAD v2: 4-69535682-G-T
• gnomAD v4: 4-68669964-G-T
• COSMIC: COSM1056874
• MyVariant Identifiers: chr4:g.69535682G>T (hg19) ; chr4:g.68669964G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68669964G>T , CM000666.2:g.68669964G>T	GRCh38
NC_000004.11:g.69535682G>T , CM000666.1:g.69535682G>T	GRCh37
NC_000004.10:g.69218277G>T	NCBI36
NG_052676.1:g.5813C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.655C>A MANE Select	ENSP00000341045.5:p.Leu219Ile
ENST00000338206.5:c.655C>A	ENSP00000341045.5:p.Leu219Ile
ENST00000616841.4:c.655C>A	ENSP00000482004.1:p.Leu219Ile
NM_001076.3:c.655C>A	NP_001067.2:p.Leu219Ile
NM_001076.4:c.655C>A MANE Select	NP_001067.2:p.Leu219Ile