Canonical Allele Identifier: CA2574470573

Gene: FH

Linked Data

• ClinVar Variation Id: 2086636
• ClinVar RCV Id: RCV003015535

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241517330T>G , CM000663.2:g.241517330T>G	GRCh38
NC_000001.10:g.241680630T>G , CM000663.1:g.241680630T>G	GRCh37
NC_000001.9:g.239747253T>G	NCBI36
NG_012338.1:g.7425A>C , LRG_504:g.7425A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.636-14A>C
ENST00000682162.1:c.162-14A>C	ENSP00000508203.1:n.162-14A>C
ENST00000682567.1:n.210-14A>C
ENST00000683521.1:c.133-14A>C	ENSP00000506864.1:n.133-14A>C
ENST00000684483.1:c.133-14A>C	ENSP00000507894.1:n.133-14A>C
ENST00000366560.4:c.133-14A>C MANE Select	ENSP00000355518.4:n.133-14A>C
ENST00000366560.3:c.133-14A>C	ENSP00000355518.3:n.133-14A>C
ENST00000493477.1:n.246-14A>C
NM_000143.3:c.133-14A>C , LRG_504t1:c.133-14A>C	NP_000134.2:n.133-14A>C
XM_011544132.1:c.-96-14A>C	XP_011542434.1:n.-96-14A>C
XM_011544132.2:c.-96-14A>C	XP_011542434.1:n.-96-14A>C
NM_000143.4:c.133-14A>C MANE Select	NP_000134.2:n.133-14A>C