Canonical Allele Identifier: CA380084368
Gene: FSHB HGNC NCBI
ARL14EP-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.30233702A>G , CM000673.2:g.30233702A>G GRCh38
NC_000011.9:g.30255249A>G , CM000673.1:g.30255249A>G GRCh37
NC_000011.8:g.30211825A>G NCBI36
NG_008144.1:g.7687A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000254122.8:c.292A>G (FSHB) ENSP00000254122.3:p.Thr98Ala
ENST00000533718.2:c.292A>G (FSHB) MANE Select ENSP00000433424.1:p.Thr98Ala
ENST00000254122.7:c.292A>G (FSHB) ENSP00000254122.3:p.Thr98Ala
ENST00000417547.1:c.292A>G (FSHB) ENSP00000416606.1:p.Thr98Ala
ENST00000533718.1:c.292A>G (FSHB) ENSP00000433424.1:p.Thr98Ala
NM_000510.2:c.292A>G (FSHB) NP_000501.1:p.Thr98Ala
NM_001018080.1:c.292A>G (FSHB) NP_001018090.1:p.Thr98Ala
XM_011519964.1:c.292A>G (FSHB) XP_011518266.1:p.Thr98Ala
XR_931152.1:n.463+83188T>C (ARL14EP-DT)
XR_931153.1:n.284+83188T>C (ARL14EP-DT)
XR_931152.2:n.463+83188T>C (ARL14EP-DT)
NM_000510.3:c.292A>G (FSHB) NP_000501.1:p.Thr98Ala
NM_001018080.2:c.292A>G (FSHB) NP_001018090.1:p.Thr98Ala
NM_000510.4:c.292A>G (FSHB) NP_000501.1:p.Thr98Ala
NM_001018080.3:c.292A>G (FSHB) NP_001018090.1:p.Thr98Ala
NM_001382289.1:c.292A>G (FSHB) MANE Select NP_001369218.1:p.Thr98Ala