Canonical Allele Identifier: CA2942729
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs756451366
gnomAD v2: 4-69535976-A-C
gnomAD v4: 4-68670258-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670258A>C , CM000666.2:g.68670258A>C GRCh38
NC_000004.11:g.69535976A>C , CM000666.1:g.69535976A>C GRCh37
NC_000004.10:g.69218571A>C NCBI36
NG_052676.1:g.5519T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.361T>G MANE Select ENSP00000341045.5:p.Tyr121Asp
ENST00000338206.5:c.361T>G ENSP00000341045.5:p.Tyr121Asp
ENST00000616841.4:c.361T>G ENSP00000482004.1:p.Tyr121Asp
NM_001076.3:c.361T>G NP_001067.2:p.Tyr121Asp
NM_001076.4:c.361T>G MANE Select NP_001067.2:p.Tyr121Asp