Canonical Allele Identifier: CA2942708
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs554358929
ExAC: 4:69535902 C / T
gnomAD v2: 4-69535902-C-T
gnomAD v3: 4-68670184-C-T
gnomAD v4: 4-68670184-C-T
MyVariant Identifiers: chr4:g.69535902C>T (hg19) chr4:g.68670184C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670184C>T , CM000666.2:g.68670184C>T GRCh38
NC_000004.11:g.69535902C>T , CM000666.1:g.69535902C>T GRCh37
NC_000004.10:g.69218497C>T NCBI36
NG_052676.1:g.5593G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.435G>A MANE Select ENSP00000341045.5:p.Lys145=
ENST00000338206.5:c.435G>A ENSP00000341045.5:p.Lys145=
ENST00000616841.4:c.435G>A ENSP00000482004.1:p.Lys145=
NM_001076.3:c.435G>A NP_001067.2:p.Lys145=
NM_001076.4:c.435G>A MANE Select NP_001067.2:p.Lys145=
Search 100 bp 5'
Search 100 bp 3'