Canonical Allele Identifier: CA98747873

Gene: UGT2B15

Linked Data

• dbSNP Id: rs376138126
• gnomAD v2: 4-69512817-T-G
• gnomAD v3: 4-68647099-T-G
• gnomAD v4: 4-68647099-T-G
• MyVariant Identifiers: chr4:g.69512817T>G (hg19) ; chr4:g.68647099T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68647099T>G , CM000666.2:g.68647099T>G	GRCh38
NC_000004.11:g.69512817T>G , CM000666.1:g.69512817T>G	GRCh37
NC_000004.10:g.69195412T>G	NCBI36
NG_052676.1:g.28678A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*5A>C MANE Select	ENSP00000341045.5:n.*5A>C
ENST00000338206.5:c.*5A>C	ENSP00000341045.5:n.*5A>C
ENST00000616841.4:c.1598A>C	ENSP00000482004.1:n.1598A>C
NM_001076.3:c.*5A>C	NP_001067.2:n.*5A>C
NM_001076.4:c.*5A>C MANE Select	NP_001067.2:n.*5A>C