Canonical Allele Identifier: CA1465883997
Gene: UGT2B10 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68817185C= , CM000666.2:g.68817185C= GRCh38
NC_000004.11:g.69682903C= , CM000666.1:g.69682903C= GRCh37
NC_000004.10:g.69717492C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265403.12:c.718+448C= MANE Select ENSP00000265403.7:n.718+448C=
ENST00000265403.11:c.718+448C= ENSP00000265403.7:n.718+448C=
ENST00000458688.2:c.466+700C= ENSP00000413420.2:n.466+700C=
NM_001075.5:c.718+448C= NP_001066.1:n.718+448C=
NM_001144767.2:c.466+700C= NP_001138239.1:n.466+700C=
NM_001290091.1:c.-26-844C= NP_001277020.1:n.-26-844C=
XM_017008585.2:c.718+448C= XP_016864074.1:n.718+448C=
NM_001075.6:c.718+448C= MANE Select NP_001066.1:n.718+448C=
NM_001144767.3:c.466+700C= NP_001138239.1:n.466+700C=
NM_001290091.2:c.-26-844C= NP_001277020.1:n.-26-844C=
Search 100 bp 5'
Search 100 bp 3'