Canonical Allele Identifier: CA797773065

Gene: UGT2B10

Linked Data

• dbSNP Id: rs1222574583
• gnomAD v3: 4-68817258-G-C
• gnomAD v4: 4-68817258-G-C
• MyVariant Identifiers: chr4:g.69682976G>C (hg19) ; chr4:g.68817258G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68817258G>C , CM000666.2:g.68817258G>C	GRCh38
NC_000004.11:g.69682976G>C , CM000666.1:g.69682976G>C	GRCh37
NC_000004.10:g.69717565G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+521G>C MANE Select	ENSP00000265403.7:n.718+521G>C
ENST00000265403.11:c.718+521G>C	ENSP00000265403.7:n.718+521G>C
ENST00000458688.2:c.467-771G>C	ENSP00000413420.2:n.467-771G>C
NM_001075.5:c.718+521G>C	NP_001066.1:n.718+521G>C
NM_001144767.2:c.467-771G>C	NP_001138239.1:n.467-771G>C
NM_001290091.1:c.-26-771G>C	NP_001277020.1:n.-26-771G>C
XM_017008585.2:c.718+521G>C	XP_016864074.1:n.718+521G>C
NM_001075.6:c.718+521G>C MANE Select	NP_001066.1:n.718+521G>C
NM_001144767.3:c.467-771G>C	NP_001138239.1:n.467-771G>C
NM_001290091.2:c.-26-771G>C	NP_001277020.1:n.-26-771G>C