Canonical Allele Identifier: CA357085611
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1283137588
gnomAD v2: 4-69535907-A-T
gnomAD v4: 4-68670189-A-T
MyVariant Identifiers: chr4:g.69535907A>T (hg19) chr4:g.68670189A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670189A>T , CM000666.2:g.68670189A>T GRCh38
NC_000004.11:g.69535907A>T , CM000666.1:g.69535907A>T GRCh37
NC_000004.10:g.69218502A>T NCBI36
NG_052676.1:g.5588T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.430T>A MANE Select ENSP00000341045.5:p.Ser144Thr
ENST00000338206.5:c.430T>A ENSP00000341045.5:p.Ser144Thr
ENST00000616841.4:c.430T>A ENSP00000482004.1:p.Ser144Thr
NM_001076.3:c.430T>A NP_001067.2:p.Ser144Thr
NM_001076.4:c.430T>A MANE Select NP_001067.2:p.Ser144Thr
Search 100 bp 5'
Search 100 bp 3'