Canonical Allele Identifier: CA15332048
Gene: UGT2B15 HGNC NCBI
MyVariant.info:
GRCh38 chr4:g.68667984T>A
GRCh37 chr4:g.69533702T>A
gnomAD v2:
4:69533702 T / A
gnomAD v3:
4:68667984 T / A
gnomAD v4:
chr4-68667984-T-A
Joint Max Group AF 0.38712246 (AMR)
Genomes Max Group AF 0.32378768 (AMR)
Exomes Max Group AF 0.40918949 (AMR)
dbSNP:
2045100
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68667984T>A , CM000666.2:g.68667984T>A GRCh38
NC_000004.11:g.69533702T>A , CM000666.1:g.69533702T>A GRCh37
NC_000004.10:g.69216297T>A NCBI36
NG_052676.1:g.7793A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.873+56A>T MANE Select ENSP00000341045.5:n.873+56A>T
ENST00000338206.5:c.873+56A>T ENSP00000341045.5:n.873+56A>T
ENST00000616841.4:c.873+56A>T ENSP00000482004.1:n.873+56A>T
NM_001076.3:c.873+56A>T NP_001067.2:n.873+56A>T
NM_001076.4:c.873+56A>T MANE Select NP_001067.2:n.873+56A>T
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