Canonical Allele Identifier: CA2670847358

Gene: UGT2B10

Linked Data

• gnomAD v4: 4-68816781-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816781G>C , CM000666.2:g.68816781G>C	GRCh38
NC_000004.11:g.69682499G>C , CM000666.1:g.69682499G>C	GRCh37
NC_000004.10:g.69717088G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+44G>C MANE Select	ENSP00000265403.7:n.718+44G>C
ENST00000265403.11:c.718+44G>C	ENSP00000265403.7:n.718+44G>C
ENST00000458688.2:c.466+296G>C	ENSP00000413420.2:n.466+296G>C
NM_001075.5:c.718+44G>C	NP_001066.1:n.718+44G>C
NM_001144767.2:c.466+296G>C	NP_001138239.1:n.466+296G>C
NM_001290091.1:c.-27+609G>C	NP_001277020.1:n.-27+609G>C
XM_017008585.2:c.718+44G>C	XP_016864074.1:n.718+44G>C
NM_001075.6:c.718+44G>C MANE Select	NP_001066.1:n.718+44G>C
NM_001144767.3:c.466+296G>C	NP_001138239.1:n.466+296G>C
NM_001290091.2:c.-27+609G>C	NP_001277020.1:n.-27+609G>C