Canonical Allele Identifier: CA1961321055
Gene: FSHB HGNC NCBI
ARL14EP-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.30230805G= , CM000673.2:g.30230805G= GRCh38
NC_000011.9:g.30252352G= , CM000673.1:g.30252352G= GRCh37
NC_000011.8:g.30208928G= NCBI36
NG_008144.1:g.4790G=

Transcript Alleles

HGVS Amino-acid Change
XM_011519964.1:c.-38+39G= (FSHB) XP_011518266.1:n.-38+39G=
XR_931152.1:n.463+86085C= (ARL14EP-DT)
XR_931153.1:n.284+86085C= (ARL14EP-DT)
XR_931152.2:n.463+86085C= (ARL14EP-DT)