Canonical Allele Identifier: CA345439216

Gene: FH

Linked Data

• ClinVar Variation Id: 2003649
• ClinVar RCV Id: RCV002811338
• MyVariant Identifiers: chr1:g.241671941T>A (hg19) ; chr1:g.241508641T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508641T>A , CM000663.2:g.241508641T>A	GRCh38
NC_000001.10:g.241671941T>A , CM000663.1:g.241671941T>A	GRCh37
NC_000001.9:g.239738564T>A	NCBI36
NG_012338.1:g.16114A>T , LRG_504:g.16114A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1203A>T
ENST00000682162.1:c.729A>T	ENSP00000508203.1:n.729A>T
ENST00000682567.1:n.777A>T
ENST00000683521.1:c.700A>T	ENSP00000506864.1:p.Thr234Ser
ENST00000684161.1:n.1915A>T
ENST00000684483.1:c.*96A>T	ENSP00000507894.1:n.*96A>T
ENST00000366560.4:c.700A>T MANE Select	ENSP00000355518.4:p.Thr234Ser
ENST00000366560.3:c.700A>T	ENSP00000355518.3:p.Thr234Ser
NM_000143.3:c.700A>T , LRG_504t1:c.700A>T	NP_000134.2:p.Thr234Ser
XM_011544132.1:c.472A>T	XP_011542434.1:p.Thr158Ser
XM_011544132.2:c.472A>T	XP_011542434.1:p.Thr158Ser
NM_000143.4:c.700A>T MANE Select	NP_000134.2:p.Thr234Ser