Canonical Allele Identifier: CA2687878765
Gene: OTUD6B HGNC NCBI

Linked Data

gnomAD v4: 8-91071043-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.91071043G>T , CM000670.2:g.91071043G>T GRCh38
NC_000008.10:g.92083271G>T , CM000670.1:g.92083271G>T GRCh37
NC_000008.9:g.92152447G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000404789.8:c.83-95G>T MANE Select ENSP00000384190.4:n.83-95G>T
ENST00000285420.8:c.173-95G>T ENSP00000285420.4:n.173-95G>T
ENST00000404789.7:c.83-95G>T ENSP00000384190.4:n.83-95G>T
ENST00000522894.5:c.83-95G>T ENSP00000428528.2:n.83-95G>T
ENST00000524027.5:n.106-95G>T
ENST00000615618.1:c.-361-95G>T ENSP00000481196.1:n.-361-95G>T
ENST00000617869.4:c.173-95G>T ENSP00000483706.1:n.173-95G>T
NM_001286745.1:c.-361-95G>T NP_001273674.1:n.-361-95G>T
NM_016023.3:c.173-95G>T NP_057107.3:n.173-95G>T
XM_011517129.1:c.173-95G>T XP_011515431.1:n.173-95G>T
NM_001286745.2:c.-361-95G>T NP_001273674.1:n.-361-95G>T
NM_016023.4:c.83-95G>T NP_057107.4:n.83-95G>T
XM_011517129.2:c.-357-95G>T XP_011515431.2:n.-357-95G>T
NM_016023.5:c.83-95G>T MANE Select NP_057107.4:n.83-95G>T
NM_001286745.3:c.-361-95G>T NP_001273674.1:n.-361-95G>T