Canonical Allele Identifier: CA357087789
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1350043262
gnomAD v2: 4-69536278-G-A
gnomAD v4: 4-68670560-G-A
MyVariant Identifiers: chr4:g.69536278G>A (hg19) chr4:g.68670560G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670560G>A , CM000666.2:g.68670560G>A GRCh38
NC_000004.11:g.69536278G>A , CM000666.1:g.69536278G>A GRCh37
NC_000004.10:g.69218873G>A NCBI36
NG_052676.1:g.5217C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.59C>T MANE Select ENSP00000341045.5:p.Ser20Phe
ENST00000338206.5:c.59C>T ENSP00000341045.5:p.Ser20Phe
ENST00000616841.4:c.59C>T ENSP00000482004.1:p.Ser20Phe
NM_001076.3:c.59C>T NP_001067.2:p.Ser20Phe
NM_001076.4:c.59C>T MANE Select NP_001067.2:p.Ser20Phe
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