Canonical Allele Identifier: CA2942801
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs770871379
ExAC: 4:69536349 C / T
gnomAD v2: 4-69536349-C-T
gnomAD v3: 4-68670631-C-T
gnomAD v4: 4-68670631-C-T
MyVariant Identifiers: chr4:g.69536349C>T (hg19) chr4:g.68670631C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670631C>T , CM000666.2:g.68670631C>T GRCh38
NC_000004.11:g.69536349C>T , CM000666.1:g.69536349C>T GRCh37
NC_000004.10:g.69218944C>T NCBI36
NG_052676.1:g.5146G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.-13G>A MANE Select ENSP00000341045.5:n.-13G>A
NM_001076.3:c.-13G>A NP_001067.2:n.-13G>A
NM_001076.4:c.-13G>A MANE Select NP_001067.2:n.-13G>A
Search 100 bp 5'
Search 100 bp 3'