Canonical Allele Identifier: CA797795750
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1197306906
gnomAD v3: 4-68670634-T-A
gnomAD v4: 4-68670634-T-A
MyVariant Identifiers: chr4:g.69536352T>A (hg19) chr4:g.68670634T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670634T>A , CM000666.2:g.68670634T>A GRCh38
NC_000004.11:g.69536352T>A , CM000666.1:g.69536352T>A GRCh37
NC_000004.10:g.69218947T>A NCBI36
NG_052676.1:g.5143A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.-16A>T MANE Select ENSP00000341045.5:n.-16A>T
NM_001076.3:c.-16A>T NP_001067.2:n.-16A>T
NM_001076.4:c.-16A>T MANE Select NP_001067.2:n.-16A>T
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