Canonical Allele Identifier: CA552612212
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1418808659
gnomAD v2: 4-69512754-A-T
gnomAD v3: 4-68647036-A-T
gnomAD v4: 4-68647036-A-T
MyVariant Identifiers: chr4:g.69512754A>T (hg19) chr4:g.68647036A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647036A>T , CM000666.2:g.68647036A>T GRCh38
NC_000004.11:g.69512754A>T , CM000666.1:g.69512754A>T GRCh37
NC_000004.10:g.69195349A>T NCBI36
NG_052676.1:g.28741T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*68T>A MANE Select ENSP00000341045.5:n.*68T>A
ENST00000338206.5:c.*68T>A ENSP00000341045.5:n.*68T>A
ENST00000616841.4:c.1661T>A ENSP00000482004.1:n.1661T>A
NM_001076.3:c.*68T>A NP_001067.2:n.*68T>A
NM_001076.4:c.*68T>A MANE Select NP_001067.2:n.*68T>A
Search 100 bp 5'
Search 100 bp 3'