Canonical Allele Identifier: CA1465884036
Gene: UGT2B10 HGNC NCBI

Linked Data

dbSNP Id: rs1737260314
gnomAD v3: 4-68817250-T-A
gnomAD v4: 4-68817250-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68817250T>A , CM000666.2:g.68817250T>A GRCh38
NC_000004.11:g.69682968T>A , CM000666.1:g.69682968T>A GRCh37
NC_000004.10:g.69717557T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265403.12:c.718+513T>A MANE Select ENSP00000265403.7:n.718+513T>A
ENST00000265403.11:c.718+513T>A ENSP00000265403.7:n.718+513T>A
ENST00000458688.2:c.466+765T>A ENSP00000413420.2:n.466+765T>A
NM_001075.5:c.718+513T>A NP_001066.1:n.718+513T>A
NM_001144767.2:c.466+765T>A NP_001138239.1:n.466+765T>A
NM_001290091.1:c.-26-779T>A NP_001277020.1:n.-26-779T>A
XM_017008585.2:c.718+513T>A XP_016864074.1:n.718+513T>A
NM_001075.6:c.718+513T>A MANE Select NP_001066.1:n.718+513T>A
NM_001144767.3:c.466+765T>A NP_001138239.1:n.466+765T>A
NM_001290091.2:c.-26-779T>A NP_001277020.1:n.-26-779T>A
Search 100 bp 5'
Search 100 bp 3'