Canonical Allele Identifier: CA2942371
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs145285645
ExAC: 4:69512912 G / T
gnomAD v2: 4-69512912-G-T
gnomAD v3: 4-68647194-G-T
gnomAD v4: 4-68647194-G-T
MyVariant Identifiers: chr4:g.69512912G>T (hg19) chr4:g.68647194G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647194G>T , CM000666.2:g.68647194G>T GRCh38
NC_000004.11:g.69512912G>T , CM000666.1:g.69512912G>T GRCh37
NC_000004.10:g.69195507G>T NCBI36
NG_052676.1:g.28583C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1503C>A MANE Select ENSP00000341045.5:p.Cys501Ter
ENST00000338206.5:c.1503C>A ENSP00000341045.5:p.Cys501Ter
ENST00000616841.4:c.1503C>A ENSP00000482004.1:p.Cys501Ter
NM_001076.3:c.1503C>A NP_001067.2:p.Cys501Ter
NM_001076.4:c.1503C>A MANE Select NP_001067.2:p.Cys501Ter
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