Canonical Allele Identifier: CA1148225110
Gene: FH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241508604T= , CM000663.2:g.241508604T= GRCh38
NC_000001.10:g.241671904T= , CM000663.1:g.241671904T= GRCh37
NC_000001.9:g.239738527T= NCBI36
NG_012338.1:g.16151A= , LRG_504:g.16151A=

Transcript Alleles

HGVS Amino-acid change
ENST00000493477.2:n.1240A=
ENST00000682162.1:c.766A= ENSP00000508203.1:n.766A=
ENST00000682567.1:n.814A=
ENST00000683521.1:c.737A= ENSP00000506864.1:p.Gln246=
ENST00000684161.1:n.1952A=
ENST00000684483.1:c.*133A= ENSP00000507894.1:n.*133A=
ENST00000366560.4:c.737A= MANE Select ENSP00000355518.4:p.Gln246=
ENST00000366560.3:c.737A= ENSP00000355518.3:p.Gln246=
NM_000143.3:c.737A= , LRG_504t1:c.737A= NP_000134.2:p.Gln246=
XM_011544132.1:c.509A= XP_011542434.1:p.Gln170=
XM_011544132.2:c.509A= XP_011542434.1:p.Gln170=
NM_000143.4:c.737A= MANE Select NP_000134.2:p.Gln246=