Canonical Allele Identifier: CA357087566
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670521-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670521T>C , CM000666.2:g.68670521T>C GRCh38
NC_000004.11:g.69536239T>C , CM000666.1:g.69536239T>C GRCh37
NC_000004.10:g.69218834T>C NCBI36
NG_052676.1:g.5256A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.98A>G MANE Select ENSP00000341045.5:p.Tyr33Cys
ENST00000338206.5:c.98A>G ENSP00000341045.5:p.Tyr33Cys
ENST00000616841.4:c.98A>G ENSP00000482004.1:p.Tyr33Cys
NM_001076.3:c.98A>G NP_001067.2:p.Tyr33Cys
NM_001076.4:c.98A>G MANE Select NP_001067.2:p.Tyr33Cys