Canonical Allele Identifier: CA345439911

Gene: FH

Linked Data

• ClinVar Variation Id: 1746359
• ClinVar RCV Id: RCV002340950
• MyVariant Identifiers: chr1:g.241675298A>C (hg19) ; chr1:g.241511998A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241511998A>C , CM000663.2:g.241511998A>C	GRCh38
NC_000001.10:g.241675298A>C , CM000663.1:g.241675298A>C	GRCh37
NC_000001.9:g.239741921A>C	NCBI36
NG_012338.1:g.12757T>G , LRG_504:g.12757T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1027T>G
ENST00000682162.1:c.553T>G	ENSP00000508203.1:n.553T>G
ENST00000682567.1:n.601T>G
ENST00000683521.1:c.524T>G	ENSP00000506864.1:p.Val175Gly
ENST00000684483.1:c.524T>G	ENSP00000507894.1:p.Val175Gly
ENST00000366560.4:c.524T>G MANE Select	ENSP00000355518.4:p.Val175Gly
ENST00000366560.3:c.524T>G	ENSP00000355518.3:p.Val175Gly
ENST00000497042.1:n.220T>G
NM_000143.3:c.524T>G , LRG_504t1:c.524T>G	NP_000134.2:p.Val175Gly
XM_011544132.1:c.296T>G	XP_011542434.1:p.Val99Gly
XM_011544132.2:c.296T>G	XP_011542434.1:p.Val99Gly
NM_000143.4:c.524T>G MANE Select	NP_000134.2:p.Val175Gly