Canonical Allele Identifier: CA98747612
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1040438069
gnomAD v3: 4-68646789-T-G
gnomAD v4: 4-68646789-T-G
MyVariant Identifiers: chr4:g.69512507T>G (hg19) chr4:g.68646789T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646789T>G , CM000666.2:g.68646789T>G GRCh38
NC_000004.11:g.69512507T>G , CM000666.1:g.69512507T>G GRCh37
NC_000004.10:g.69195102T>G NCBI36
NG_052676.1:g.28988A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*315A>C MANE Select ENSP00000341045.5:n.*315A>C
ENST00000338206.5:c.*315A>C ENSP00000341045.5:n.*315A>C
ENST00000616841.4:c.1732+176A>C ENSP00000482004.1:n.1732+176A>C
NM_001076.3:c.*315A>C NP_001067.2:n.*315A>C
NM_001076.4:c.*315A>C MANE Select NP_001067.2:n.*315A>C
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