Canonical Allele Identifier: CA1229578176
Gene: FH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241502570C= , CM000663.2:g.241502570C= GRCh38
NC_000001.10:g.241665870C= , CM000663.1:g.241665870C= GRCh37
NC_000001.9:g.239732493C= NCBI36
NG_012338.1:g.22185G= , LRG_504:g.22185G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000493477.2:n.1612G=
ENST00000682162.1:c.1138G= ENSP00000508203.1:n.1138G=
ENST00000682567.1:n.2657G=
ENST00000683521.1:c.1109G= ENSP00000506864.1:p.Gly370=
ENST00000684161.1:n.2324G=
ENST00000684483.1:c.*505G= ENSP00000507894.1:n.*505G=
ENST00000366560.4:c.1109G= MANE Select ENSP00000355518.4:p.Gly370=
ENST00000366560.3:c.1109G= ENSP00000355518.3:p.Gly370=
NM_000143.3:c.1109G= , LRG_504t1:c.1109G= NP_000134.2:p.Gly370=
XM_011544132.1:c.881G= XP_011542434.1:p.Gly294=
XM_011544132.2:c.881G= XP_011542434.1:p.Gly294=
NM_000143.4:c.1109G= MANE Select NP_000134.2:p.Gly370=