Canonical Allele Identifier: CA345442002

Gene: FH

Linked Data

• ClinVar Variation Id: 964063
• ClinVar RCV Id: RCV002567915 ; RCV003380923
• dbSNP Id: rs543844061
• MyVariant Identifiers: chr1:g.241680595T>C (hg19) ; chr1:g.241517295T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241517295T>C , CM000663.2:g.241517295T>C	GRCh38
NC_000001.10:g.241680595T>C , CM000663.1:g.241680595T>C	GRCh37
NC_000001.9:g.239747218T>C	NCBI36
NG_012338.1:g.7460A>G , LRG_504:g.7460A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.657A>G
ENST00000682162.1:c.183A>G	ENSP00000508203.1:p.Gly61=
ENST00000682567.1:n.231A>G
ENST00000683521.1:c.154A>G	ENSP00000506864.1:p.Ile52Val
ENST00000684483.1:c.154A>G	ENSP00000507894.1:p.Ile52Val
ENST00000366560.4:c.154A>G MANE Select	ENSP00000355518.4:p.Ile52Val
ENST00000366560.3:c.154A>G	ENSP00000355518.3:p.Ile52Val
ENST00000493477.1:n.267A>G
NM_000143.3:c.154A>G , LRG_504t1:c.154A>G	NP_000134.2:p.Ile52Val
XM_011544132.1:c.-75A>G	XP_011542434.1:n.-75A>G
XM_011544132.2:c.-75A>G	XP_011542434.1:n.-75A>G
NM_000143.4:c.154A>G MANE Select	NP_000134.2:p.Ile52Val