Canonical Allele Identifier: CA797795832

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1281014419
• gnomAD v3: 4-68670751-CT-C
• gnomAD v4: 4-68670751-CT-C
• MyVariant Identifiers: chr4:g.69536470del (hg19) ; chr4:g.68670752del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670752del , CM000666.2:g.68670752del	GRCh38
NC_000004.11:g.69536470del , CM000666.1:g.69536470del	GRCh37
NC_000004.10:g.69219065del	NCBI36
NG_052676.1:g.5025del

Transcript Alleles

HGVS	Amino-acid Change
NM_001076.3:c.-134del	NP_001067.2:n.-134del