Canonical Allele Identifier: CA424076290

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241675327T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512027T>C , CM000663.2:g.241512027T>C	GRCh38
NC_000001.10:g.241675327T>C , CM000663.1:g.241675327T>C	GRCh37
NC_000001.9:g.239741950T>C	NCBI36
NG_012338.1:g.12728A>G , LRG_504:g.12728A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.998A>G
ENST00000682162.1:c.524A>G	ENSP00000508203.1:n.524A>G
ENST00000682567.1:n.572A>G
ENST00000683521.1:c.495A>G	ENSP00000506864.1:p.Leu165=
ENST00000684483.1:c.495A>G	ENSP00000507894.1:p.Leu165=
ENST00000366560.4:c.495A>G MANE Select	ENSP00000355518.4:p.Leu165=
ENST00000366560.3:c.495A>G	ENSP00000355518.3:p.Leu165=
ENST00000497042.1:n.191A>G
NM_000143.3:c.495A>G , LRG_504t1:c.495A>G	NP_000134.2:p.Leu165=
XM_011544132.1:c.267A>G	XP_011542434.1:p.Leu89=
XM_011544132.2:c.267A>G	XP_011542434.1:p.Leu89=
NM_000143.4:c.495A>G MANE Select	NP_000134.2:p.Leu165=