Canonical Allele Identifier: CA357082995
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69512870A>C (hg19) chr4:g.68647152A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647152A>C , CM000666.2:g.68647152A>C GRCh38
NC_000004.11:g.69512870A>C , CM000666.1:g.69512870A>C GRCh37
NC_000004.10:g.69195465A>C NCBI36
NG_052676.1:g.28625T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1545T>G MANE Select ENSP00000341045.5:p.Phe515Leu
ENST00000338206.5:c.1545T>G ENSP00000341045.5:p.Phe515Leu
ENST00000616841.4:c.1545T>G ENSP00000482004.1:p.Phe515Leu
NM_001076.3:c.1545T>G NP_001067.2:p.Phe515Leu
NM_001076.4:c.1545T>G MANE Select NP_001067.2:p.Phe515Leu
Search 100 bp 5'
Search 100 bp 3'