Canonical Allele Identifier: CA357082982

Gene: UGT2B15

Linked Data

• MyVariant Identifiers: chr4:g.69512865A>G (hg19) ; chr4:g.68647147A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68647147A>G , CM000666.2:g.68647147A>G	GRCh38
NC_000004.11:g.69512865A>G , CM000666.1:g.69512865A>G	GRCh37
NC_000004.10:g.69195460A>G	NCBI36
NG_052676.1:g.28630T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.1550T>C MANE Select	ENSP00000341045.5:p.Phe517Ser
ENST00000338206.5:c.1550T>C	ENSP00000341045.5:p.Phe517Ser
ENST00000616841.4:c.1550T>C	ENSP00000482004.1:p.Phe517Ser
NM_001076.3:c.1550T>C	NP_001067.2:p.Phe517Ser
NM_001076.4:c.1550T>C MANE Select	NP_001067.2:p.Phe517Ser