Canonical Allele Identifier: CA439935252
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69535887C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670169C>G , CM000666.2:g.68670169C>G GRCh38
NC_000004.11:g.69535887C>G , CM000666.1:g.69535887C>G GRCh37
NC_000004.10:g.69218482C>G NCBI36
NG_052676.1:g.5608G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.450G>C MANE Select ENSP00000341045.5:p.Leu150=
ENST00000338206.5:c.450G>C ENSP00000341045.5:p.Leu150=
ENST00000616841.4:c.450G>C ENSP00000482004.1:p.Leu150=
NM_001076.3:c.450G>C NP_001067.2:p.Leu150=
NM_001076.4:c.450G>C MANE Select NP_001067.2:p.Leu150=