Canonical Allele Identifier: CA1229580580
Gene: FH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241508522A= , CM000663.2:g.241508522A= GRCh38
NC_000001.10:g.241671822A= , CM000663.1:g.241671822A= GRCh37
NC_000001.9:g.239738445A= NCBI36
NG_012338.1:g.16233T= , LRG_504:g.16233T=

Transcript Alleles

HGVS Amino-acid change
ENST00000493477.2:n.1241+81T=
ENST00000682162.1:c.767+81T= ENSP00000508203.1:n.767+81T=
ENST00000682567.1:n.815+81T=
ENST00000683521.1:c.738+81T= ENSP00000506864.1:n.738+81T=
ENST00000684161.1:n.1953+81T=
ENST00000684483.1:c.*134+81T= ENSP00000507894.1:n.*134+81T=
ENST00000366560.4:c.738+81T= MANE Select ENSP00000355518.4:n.738+81T=
ENST00000366560.3:c.738+81T= ENSP00000355518.3:n.738+81T=
NM_000143.3:c.738+81T= , LRG_504t1:c.738+81T= NP_000134.2:n.738+81T=
XM_011544132.1:c.510+81T= XP_011542434.1:n.510+81T=
XM_011544132.2:c.510+81T= XP_011542434.1:n.510+81T=
NM_000143.4:c.738+81T= MANE Select NP_000134.2:n.738+81T=