Canonical Allele Identifier: CA357082979

Gene: UGT2B15

Linked Data

• MyVariant Identifiers: chr4:g.69512864G>C (hg19) ; chr4:g.68647146G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68647146G>C , CM000666.2:g.68647146G>C	GRCh38
NC_000004.11:g.69512864G>C , CM000666.1:g.69512864G>C	GRCh37
NC_000004.10:g.69195459G>C	NCBI36
NG_052676.1:g.28631C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.1551C>G MANE Select	ENSP00000341045.5:p.Phe517Leu
ENST00000338206.5:c.1551C>G	ENSP00000341045.5:p.Phe517Leu
ENST00000616841.4:c.1551C>G	ENSP00000482004.1:p.Phe517Leu
NM_001076.3:c.1551C>G	NP_001067.2:p.Phe517Leu
NM_001076.4:c.1551C>G MANE Select	NP_001067.2:p.Phe517Leu