Canonical Allele Identifier: CA552177711

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1340851527
• gnomAD v2: 4-69512314-A-G
• gnomAD v3: 4-68646596-A-G
• gnomAD v4: 4-68646596-A-G
• MyVariant Identifiers: chr4:g.69512314A>G (hg19) ; chr4:g.68646596A>G (hg38)

Genomic Alleles

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

Transcript Alleles

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