Canonical Allele Identifier: CA11725795

Gene: UGT2B15

Linked Data

• dbSNP Id: rs35791822
• gnomAD v2: 4-69512595-C-A
• gnomAD v3: 4-68646877-C-A
• gnomAD v4: 4-68646877-C-A
• MyVariant Identifiers: chr4:g.69512595C>A (hg19) ; chr4:g.68646877C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646877C>A , CM000666.2:g.68646877C>A	GRCh38
NC_000004.11:g.69512595C>A , CM000666.1:g.69512595C>A	GRCh37
NC_000004.10:g.69195190C>A	NCBI36
NG_052676.1:g.28900G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*227G>T MANE Select	ENSP00000341045.5:n.*227G>T
ENST00000338206.5:c.*227G>T	ENSP00000341045.5:n.*227G>T
ENST00000616841.4:c.1732+88G>T	ENSP00000482004.1:n.1732+88G>T
NM_001076.3:c.*227G>T	NP_001067.2:n.*227G>T
NM_001076.4:c.*227G>T MANE Select	NP_001067.2:n.*227G>T