Canonical Allele Identifier: CA345437331

Gene: FH

Linked Data

• ClinVar Variation Id: 1068226
• ClinVar RCV Id: RCV003104060
• dbSNP Id: rs886039366
• MyVariant Identifiers: chr1:g.241665774T>A (hg19) ; chr1:g.241502474T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502474T>A , CM000663.2:g.241502474T>A	GRCh38
NC_000001.10:g.241665774T>A , CM000663.1:g.241665774T>A	GRCh37
NC_000001.9:g.239732397T>A	NCBI36
NG_012338.1:g.22281A>T , LRG_504:g.22281A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1708A>T
ENST00000682162.1:c.1234A>T	ENSP00000508203.1:n.1234A>T
ENST00000682567.1:n.2753A>T
ENST00000683521.1:c.1205A>T	ENSP00000506864.1:p.His402Leu
ENST00000684161.1:n.2420A>T
ENST00000684483.1:c.*601A>T	ENSP00000507894.1:n.*601A>T
ENST00000366560.4:c.1205A>T MANE Select	ENSP00000355518.4:p.His402Leu
ENST00000366560.3:c.1205A>T	ENSP00000355518.3:p.His402Leu
NM_000143.3:c.1205A>T , LRG_504t1:c.1205A>T	NP_000134.2:p.His402Leu
XM_011544132.1:c.977A>T	XP_011542434.1:p.His326Leu
XM_011544132.2:c.977A>T	XP_011542434.1:p.His326Leu
NM_000143.4:c.1205A>T MANE Select	NP_000134.2:p.His402Leu