Canonical Allele Identifier: CA98787667

Gene: UGT2B10

Linked Data

• dbSNP Id: rs942805018
• gnomAD v2: 4-69682824-T-C
• gnomAD v3: 4-68817106-T-C
• gnomAD v4: 4-68817106-T-C
• MyVariant Identifiers: chr4:g.69682824T>C (hg19) ; chr4:g.68817106T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68817106T>C , CM000666.2:g.68817106T>C	GRCh38
NC_000004.11:g.69682824T>C , CM000666.1:g.69682824T>C	GRCh37
NC_000004.10:g.69717413T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265403.12:c.718+369T>C MANE Select	ENSP00000265403.7:n.718+369T>C
ENST00000265403.11:c.718+369T>C	ENSP00000265403.7:n.718+369T>C
ENST00000458688.2:c.466+621T>C	ENSP00000413420.2:n.466+621T>C
NM_001075.5:c.718+369T>C	NP_001066.1:n.718+369T>C
NM_001144767.2:c.466+621T>C	NP_001138239.1:n.466+621T>C
NM_001290091.1:c.-26-923T>C	NP_001277020.1:n.-26-923T>C
XM_017008585.2:c.718+369T>C	XP_016864074.1:n.718+369T>C
NM_001075.6:c.718+369T>C MANE Select	NP_001066.1:n.718+369T>C
NM_001144767.3:c.466+621T>C	NP_001138239.1:n.466+621T>C
NM_001290091.2:c.-26-923T>C	NP_001277020.1:n.-26-923T>C