Canonical Allele Identifier: CA1229577314
Gene: FH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241500573G= , CM000663.2:g.241500573G= GRCh38
NC_000001.10:g.241663873G= , CM000663.1:g.241663873G= GRCh37
NC_000001.9:g.239730496G= NCBI36
NG_012338.1:g.24182C= , LRG_504:g.24182C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000493477.2:n.1757C=
ENST00000682162.1:c.1283C= ENSP00000508203.1:n.1283C=
ENST00000682567.1:n.4654C=
ENST00000683521.1:c.1254C= ENSP00000506864.1:p.His418=
ENST00000684161.1:n.2469C=
ENST00000684483.1:c.*650C= ENSP00000507894.1:n.*650C=
ENST00000366560.4:c.1254C= MANE Select ENSP00000355518.4:p.His418=
ENST00000366560.3:c.1254C= ENSP00000355518.3:p.His418=
NM_000143.3:c.1254C= , LRG_504t1:c.1254C= NP_000134.2:p.His418=
XM_011544132.1:c.1026C= XP_011542434.1:p.His342=
XM_011544132.2:c.1026C= XP_011542434.1:p.His342=
NM_000143.4:c.1254C= MANE Select NP_000134.2:p.His418=