Canonical Allele Identifier: CA2942805
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs770130346
ExAC: 4:69536362 C / T
gnomAD v2: 4-69536362-C-T
gnomAD v4: 4-68670644-C-T
MyVariant Identifiers: chr4:g.69536362C>T (hg19) chr4:g.68670644C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670644C>T , CM000666.2:g.68670644C>T GRCh38
NC_000004.11:g.69536362C>T , CM000666.1:g.69536362C>T GRCh37
NC_000004.10:g.69218957C>T NCBI36
NG_052676.1:g.5133G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.-26G>A MANE Select ENSP00000341045.5:n.-26G>A
NM_001076.3:c.-26G>A NP_001067.2:n.-26G>A
NM_001076.4:c.-26G>A MANE Select NP_001067.2:n.-26G>A
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