Canonical Allele Identifier: CA552185663
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1310184702
gnomAD v2: 4-69536343-C-A
gnomAD v4: 4-68670625-C-A
MyVariant Identifiers: chr4:g.69536343C>A (hg19) chr4:g.68670625C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670625C>A , CM000666.2:g.68670625C>A GRCh38
NC_000004.11:g.69536343C>A , CM000666.1:g.69536343C>A GRCh37
NC_000004.10:g.69218938C>A NCBI36
NG_052676.1:g.5152G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.-7G>T MANE Select ENSP00000341045.5:n.-7G>T
ENST00000338206.5:c.-7G>T ENSP00000341045.5:n.-7G>T
NM_001076.3:c.-7G>T NP_001067.2:n.-7G>T
NM_001076.4:c.-7G>T MANE Select NP_001067.2:n.-7G>T
Search 100 bp 5'
Search 100 bp 3'