Canonical Allele Identifier: CA552177803

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1490841808
• gnomAD v2: 4-69512554-T-C
• gnomAD v3: 4-68646836-T-C
• gnomAD v4: 4-68646836-T-C
• MyVariant Identifiers: chr4:g.69512554T>C (hg19) ; chr4:g.68646836T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646836T>C , CM000666.2:g.68646836T>C	GRCh38
NC_000004.11:g.69512554T>C , CM000666.1:g.69512554T>C	GRCh37
NC_000004.10:g.69195149T>C	NCBI36
NG_052676.1:g.28941A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*268A>G MANE Select	ENSP00000341045.5:n.*268A>G
ENST00000338206.5:c.*268A>G	ENSP00000341045.5:n.*268A>G
ENST00000616841.4:c.1732+129A>G	ENSP00000482004.1:n.1732+129A>G
NM_001076.3:c.*268A>G	NP_001067.2:n.*268A>G
NM_001076.4:c.*268A>G MANE Select	NP_001067.2:n.*268A>G