Canonical Allele Identifier: CA357085903

Gene: UGT2B15

Linked Data

• MyVariant Identifiers: chr4:g.69535958G>C (hg19) ; chr4:g.68670240G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670240G>C , CM000666.2:g.68670240G>C	GRCh38
NC_000004.11:g.69535958G>C , CM000666.1:g.69535958G>C	GRCh37
NC_000004.10:g.69218553G>C	NCBI36
NG_052676.1:g.5537C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.379C>G MANE Select	ENSP00000341045.5:p.Leu127Val
ENST00000338206.5:c.379C>G	ENSP00000341045.5:p.Leu127Val
ENST00000616841.4:c.379C>G	ENSP00000482004.1:p.Leu127Val
NM_001076.3:c.379C>G	NP_001067.2:p.Leu127Val
NM_001076.4:c.379C>G MANE Select	NP_001067.2:p.Leu127Val