Canonical Allele Identifier: CA2942360

Gene: UGT2B15

Linked Data

• dbSNP Id: rs565300452
• ExAC: 4:69512872 A / G
• gnomAD v2: 4-69512872-A-G
• gnomAD v3: 4-68647154-A-G
• gnomAD v4: 4-68647154-A-G
• MyVariant Identifiers: chr4:g.69512872A>G (hg19) ; chr4:g.68647154A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68647154A>G , CM000666.2:g.68647154A>G	GRCh38
NC_000004.11:g.69512872A>G , CM000666.1:g.69512872A>G	GRCh37
NC_000004.10:g.69195467A>G	NCBI36
NG_052676.1:g.28623T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.1543T>C MANE Select	ENSP00000341045.5:p.Phe515Leu
ENST00000338206.5:c.1543T>C	ENSP00000341045.5:p.Phe515Leu
ENST00000616841.4:c.1543T>C	ENSP00000482004.1:p.Phe515Leu
NM_001076.3:c.1543T>C	NP_001067.2:p.Phe515Leu
NM_001076.4:c.1543T>C MANE Select	NP_001067.2:p.Phe515Leu