Canonical Allele Identifier: CA13045020
Gene: TTC39B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs471364

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15289580C>T , CM000671.2:g.15289580C>T GRCh38
NC_000009.11:g.15289578C>T , CM000671.1:g.15289578C>T GRCh37
NC_000009.10:g.15279578C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001168339.1:c.240+17504G>A VV NP_001161811.1:p.=
NM_001168340.1:c.240+17504G>A VV NP_001161812.1:p.=
NM_001168341.1:c.240+17504G>A VV NP_001161813.1:p.=
NM_152574.2:c.240+17504G>A VV NP_689787.2:p.=
XM_011517733.1:c.240+17504G>A XP_011516035.1:p.=
XM_017014310.1:c.-113+9770G>A XP_016869799.1:p.=
XM_017014311.1:c.-222+9770G>A XP_016869800.1:p.=
XM_024447422.1:c.-52+9770G>A XP_024303190.1:p.=
XR_001746190.1:n.277+17504G>A
ENST00000297615.9:c.240+17504G>A ENSP00000297615.5:p.=
ENST00000380850.8:c.240+17504G>A ENSP00000370231.4:p.=
ENST00000505732.5:n.277+17504G>A
ENST00000506891.1:n.126+17504G>A ENSP00000427314.1:p.=
ENST00000512701.6:c.240+17504G>A ENSP00000422496.1:p.=