Canonical Allele Identifier: CA2942644

Gene: UGT2B15

Linked Data

• dbSNP Id: rs751411220
• ExAC: 4:69535581 C / A
• gnomAD v2: 4-69535581-C-A
• gnomAD v3: 4-68669863-C-A
• gnomAD v4: 4-68669863-C-A
• MyVariant Identifiers: chr4:g.69535581C>A (hg19) ; chr4:g.68669863C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68669863C>A , CM000666.2:g.68669863C>A	GRCh38
NC_000004.11:g.69535581C>A , CM000666.1:g.69535581C>A	GRCh37
NC_000004.10:g.69218176C>A	NCBI36
NG_052676.1:g.5914G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.724+32G>T MANE Select	ENSP00000341045.5:n.724+32G>T
ENST00000338206.5:c.724+32G>T	ENSP00000341045.5:n.724+32G>T
ENST00000616841.4:c.724+32G>T	ENSP00000482004.1:n.724+32G>T
NM_001076.3:c.724+32G>T	NP_001067.2:n.724+32G>T
NM_001076.4:c.724+32G>T MANE Select	NP_001067.2:n.724+32G>T