Canonical Allele Identifier: CA2942736
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs765332840
gnomAD v2: 4-69535997-G-A
gnomAD v3: 4-68670279-G-A
gnomAD v4: 4-68670279-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670279G>A , CM000666.2:g.68670279G>A GRCh38
NC_000004.11:g.69535997G>A , CM000666.1:g.69535997G>A GRCh37
NC_000004.10:g.69218592G>A NCBI36
NG_052676.1:g.5498C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.340C>T MANE Select ENSP00000341045.5:p.Gln114Ter
ENST00000338206.5:c.340C>T ENSP00000341045.5:p.Gln114Ter
ENST00000616841.4:c.340C>T ENSP00000482004.1:p.Gln114Ter
NM_001076.3:c.340C>T NP_001067.2:p.Gln114Ter
NM_001076.4:c.340C>T MANE Select NP_001067.2:p.Gln114Ter