Canonical Allele Identifier: CA357082997

Gene: UGT2B15

Linked Data

• MyVariant Identifiers: chr4:g.69512871A>C (hg19) ; chr4:g.68647153A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68647153A>C , CM000666.2:g.68647153A>C	GRCh38
NC_000004.11:g.69512871A>C , CM000666.1:g.69512871A>C	GRCh37
NC_000004.10:g.69195466A>C	NCBI36
NG_052676.1:g.28624T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.1544T>G MANE Select	ENSP00000341045.5:p.Phe515Cys
ENST00000338206.5:c.1544T>G	ENSP00000341045.5:p.Phe515Cys
ENST00000616841.4:c.1544T>G	ENSP00000482004.1:p.Phe515Cys
NM_001076.3:c.1544T>G	NP_001067.2:p.Phe515Cys
NM_001076.4:c.1544T>G MANE Select	NP_001067.2:p.Phe515Cys