Canonical Allele Identifier: CA797777115

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1340851527
• gnomAD v3: 4-68646596-A-T
• gnomAD v4: 4-68646596-A-T
• MyVariant Identifiers: chr4:g.69512314A>T (hg19) ; chr4:g.68646596A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646596A>T , CM000666.2:g.68646596A>T	GRCh38
NC_000004.11:g.69512314A>T , CM000666.1:g.69512314A>T	GRCh37
NC_000004.10:g.69194909A>T	NCBI36
NG_052676.1:g.29181T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000616841.4:c.1732+369T>A	ENSP00000482004.1:n.1732+369T>A