Canonical Allele Identifier: CA2739274059

Gene: FH

Linked Data

• ClinVar Variation Id: 2871383
• ClinVar RCV Id: RCV003698443

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241517321A>G , CM000663.2:g.241517321A>G	GRCh38
NC_000001.10:g.241680621A>G , CM000663.1:g.241680621A>G	GRCh37
NC_000001.9:g.239747244A>G	NCBI36
NG_012338.1:g.7434T>C , LRG_504:g.7434T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.636-5T>C
ENST00000682162.1:c.162-5T>C	ENSP00000508203.1:n.162-5T>C
ENST00000682567.1:n.210-5T>C
ENST00000683521.1:c.133-5T>C	ENSP00000506864.1:n.133-5T>C
ENST00000684483.1:c.133-5T>C	ENSP00000507894.1:n.133-5T>C
ENST00000366560.4:c.133-5T>C MANE Select	ENSP00000355518.4:n.133-5T>C
ENST00000366560.3:c.133-5T>C	ENSP00000355518.3:n.133-5T>C
ENST00000493477.1:n.246-5T>C
NM_000143.3:c.133-5T>C , LRG_504t1:c.133-5T>C	NP_000134.2:n.133-5T>C
XM_011544132.1:c.-96-5T>C	XP_011542434.1:n.-96-5T>C
XM_011544132.2:c.-96-5T>C	XP_011542434.1:n.-96-5T>C
NM_000143.4:c.133-5T>C MANE Select	NP_000134.2:n.133-5T>C