Canonical Allele Identifier: CA439935229
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69535869G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670151G>C , CM000666.2:g.68670151G>C GRCh38
NC_000004.11:g.69535869G>C , CM000666.1:g.69535869G>C GRCh37
NC_000004.10:g.69218464G>C NCBI36
NG_052676.1:g.5626C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.468C>G MANE Select ENSP00000341045.5:p.Pro156=
ENST00000338206.5:c.468C>G ENSP00000341045.5:p.Pro156=
ENST00000616841.4:c.468C>G ENSP00000482004.1:p.Pro156=
NM_001076.3:c.468C>G NP_001067.2:p.Pro156=
NM_001076.4:c.468C>G MANE Select NP_001067.2:p.Pro156=
Search 100 bp 5'
Search 100 bp 3'