Canonical Allele Identifier: CA98747785
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs776790647
gnomAD v2: 4-69512776-G-T
gnomAD v4: 4-68647058-G-T
MyVariant Identifiers: chr4:g.69512776G>T (hg19) chr4:g.68647058G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647058G>T , CM000666.2:g.68647058G>T GRCh38
NC_000004.11:g.69512776G>T , CM000666.1:g.69512776G>T GRCh37
NC_000004.10:g.69195371G>T NCBI36
NG_052676.1:g.28719C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*46C>A MANE Select ENSP00000341045.5:n.*46C>A
ENST00000338206.5:c.*46C>A ENSP00000341045.5:n.*46C>A
ENST00000616841.4:c.1639C>A ENSP00000482004.1:n.1639C>A
NM_001076.3:c.*46C>A NP_001067.2:n.*46C>A
NM_001076.4:c.*46C>A MANE Select NP_001067.2:n.*46C>A
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