Canonical Allele Identifier: CA98791051
Community Standard Title: NM_001075.6(UGT2B10):c.868-2A>C
Gene: UGT2B10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68822269A>C , CM000666.2:g.68822269A>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
NM_001075.6:c.868-2A>C MANE Select NP_001066.1:n.868-2A>C
ENST00000265403.12:c.868-2A>C MANE Select ENSP00000265403.7:n.868-2A>C
NM_001075.5:c.868-2A>C NP_001066.1:n.868-2A>C
NM_001144767.2:c.616-2A>C NP_001138239.1:n.616-2A>C
NM_001144767.3:c.616-2A>C NP_001138239.1:n.616-2A>C
NM_001290091.1:c.124-2A>C NP_001277020.1:n.124-2A>C
NM_001290091.2:c.124-2A>C NP_001277020.1:n.124-2A>C
ENST00000265403.11:c.868-2A>C ENSP00000265403.7:n.868-2A>C
ENST00000458688.2:c.616-2A>C ENSP00000413420.2:n.616-2A>C
XM_017008585.2:c.868-11A>C XP_016864074.1:n.868-11A>C