Canonical Allele Identifier: CA2942703
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs530442418
gnomAD v2: 4-69535892-T-G
gnomAD v3: 4-68670174-T-G
gnomAD v4: 4-68670174-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670174T>G , CM000666.2:g.68670174T>G GRCh38
NC_000004.11:g.69535892T>G , CM000666.1:g.69535892T>G GRCh37
NC_000004.10:g.69218487T>G NCBI36
NG_052676.1:g.5603A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.445A>C MANE Select ENSP00000341045.5:p.Ile149Leu
ENST00000338206.5:c.445A>C ENSP00000341045.5:p.Ile149Leu
ENST00000616841.4:c.445A>C ENSP00000482004.1:p.Ile149Leu
NM_001076.3:c.445A>C NP_001067.2:p.Ile149Leu
NM_001076.4:c.445A>C MANE Select NP_001067.2:p.Ile149Leu