Canonical Allele Identifier: CA357086251
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733270020
gnomAD v4: 4-68670292-A-T
MyVariant Identifiers: chr4:g.69536010A>T (hg19) chr4:g.68670292A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670292A>T , CM000666.2:g.68670292A>T GRCh38
NC_000004.11:g.69536010A>T , CM000666.1:g.69536010A>T GRCh37
NC_000004.10:g.69218605A>T NCBI36
NG_052676.1:g.5485T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.327T>A MANE Select ENSP00000341045.5:p.Tyr109Ter
ENST00000338206.5:c.327T>A ENSP00000341045.5:p.Tyr109Ter
ENST00000616841.4:c.327T>A ENSP00000482004.1:p.Tyr109Ter
NM_001076.3:c.327T>A NP_001067.2:p.Tyr109Ter
NM_001076.4:c.327T>A MANE Select NP_001067.2:p.Tyr109Ter
Search 100 bp 5'
Search 100 bp 3'