Canonical Allele Identifier: CA552177725
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1194163315
gnomAD v2: 4-69512352-T-G
MyVariant Identifiers: chr4:g.69512352T>G (hg19) chr4:g.68646634T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646634T>G , CM000666.2:g.68646634T>G GRCh38
NC_000004.11:g.69512352T>G , CM000666.1:g.69512352T>G GRCh37
NC_000004.10:g.69194947T>G NCBI36
NG_052676.1:g.29143A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*470A>C MANE Select ENSP00000341045.5:n.*470A>C
ENST00000338206.5:c.*470A>C ENSP00000341045.5:n.*470A>C
ENST00000616841.4:c.1732+331A>C ENSP00000482004.1:n.1732+331A>C
NM_001076.3:c.*470A>C NP_001067.2:n.*470A>C
NM_001076.4:c.*470A>C MANE Select NP_001067.2:n.*470A>C
Search 100 bp 5'
Search 100 bp 3'