Canonical Allele Identifier: CA797795778
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs187647606
gnomAD v3: 4-68670647-G-A
gnomAD v4: 4-68670647-G-A
MyVariant Identifiers: chr4:g.69536365G>A (hg19) chr4:g.68670647G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670647G>A , CM000666.2:g.68670647G>A GRCh38
NC_000004.11:g.69536365G>A , CM000666.1:g.69536365G>A GRCh37
NC_000004.10:g.69218960G>A NCBI36
NG_052676.1:g.5130C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.-29C>T MANE Select ENSP00000341045.5:n.-29C>T
NM_001076.3:c.-29C>T NP_001067.2:n.-29C>T
NM_001076.4:c.-29C>T MANE Select NP_001067.2:n.-29C>T
Search 100 bp 5'
Search 100 bp 3'