Canonical Allele Identifier: CA98759656
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs556569318
gnomAD v2: 4-69535512-C-G
gnomAD v3: 4-68669794-C-G
gnomAD v4: 4-68669794-C-G
MyVariant Identifiers: chr4:g.69535512C>G (hg19) chr4:g.68669794C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669794C>G , CM000666.2:g.68669794C>G GRCh38
NC_000004.11:g.69535512C>G , CM000666.1:g.69535512C>G GRCh37
NC_000004.10:g.69218107C>G NCBI36
NG_052676.1:g.5983G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+101G>C MANE Select ENSP00000341045.5:n.724+101G>C
ENST00000338206.5:c.724+101G>C ENSP00000341045.5:n.724+101G>C
ENST00000616841.4:c.724+101G>C ENSP00000482004.1:n.724+101G>C
NM_001076.3:c.724+101G>C NP_001067.2:n.724+101G>C
NM_001076.4:c.724+101G>C MANE Select NP_001067.2:n.724+101G>C
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