Canonical Allele Identifier: CA2942367
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs139372148
ExAC: 4:69512895 A / G
gnomAD v2: 4-69512895-A-G
MyVariant Identifiers: chr4:g.69512895A>G (hg19) chr4:g.68647177A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647177A>G , CM000666.2:g.68647177A>G GRCh38
NC_000004.11:g.69512895A>G , CM000666.1:g.69512895A>G GRCh37
NC_000004.10:g.69195490A>G NCBI36
NG_052676.1:g.28600T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1520T>C MANE Select ENSP00000341045.5:p.Phe507Ser
ENST00000338206.5:c.1520T>C ENSP00000341045.5:p.Phe507Ser
ENST00000616841.4:c.1520T>C ENSP00000482004.1:p.Phe507Ser
NM_001076.3:c.1520T>C NP_001067.2:p.Phe507Ser
NM_001076.4:c.1520T>C MANE Select NP_001067.2:p.Phe507Ser
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