Canonical Allele Identifier: CA2942669
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs772502374
gnomAD v2: 4-69535702-A-G
gnomAD v3: 4-68669984-A-G
gnomAD v4: 4-68669984-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669984A>G , CM000666.2:g.68669984A>G GRCh38
NC_000004.11:g.69535702A>G , CM000666.1:g.69535702A>G GRCh37
NC_000004.10:g.69218297A>G NCBI36
NG_052676.1:g.5793T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.635T>C MANE Select ENSP00000341045.5:p.Ile212Thr
ENST00000338206.5:c.635T>C ENSP00000341045.5:p.Ile212Thr
ENST00000616841.4:c.635T>C ENSP00000482004.1:p.Ile212Thr
NM_001076.3:c.635T>C NP_001067.2:p.Ile212Thr
NM_001076.4:c.635T>C MANE Select NP_001067.2:p.Ile212Thr