Canonical Allele Identifier: CA345438259

Gene: FH

Linked Data

• ClinVar Variation Id: 2681942
• ClinVar RCV Id: RCV003477234
• dbSNP Id: rs2147916201
• MyVariant Identifiers: chr1:g.241667455G>A (hg19) ; chr1:g.241504155G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504155G>A , CM000663.2:g.241504155G>A	GRCh38
NC_000001.10:g.241667455G>A , CM000663.1:g.241667455G>A	GRCh37
NC_000001.9:g.239734078G>A	NCBI36
NG_012338.1:g.20600C>T , LRG_504:g.20600C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1498C>T
ENST00000682162.1:c.1024C>T	ENSP00000508203.1:n.1024C>T
ENST00000682567.1:n.1072C>T
ENST00000683521.1:c.995C>T	ENSP00000506864.1:p.Ala332Val
ENST00000684161.1:n.2210C>T
ENST00000684483.1:c.*391C>T	ENSP00000507894.1:n.*391C>T
ENST00000366560.4:c.995C>T MANE Select	ENSP00000355518.4:p.Ala332Val
ENST00000366560.3:c.995C>T	ENSP00000355518.3:p.Ala332Val
NM_000143.3:c.995C>T , LRG_504t1:c.995C>T	NP_000134.2:p.Ala332Val
XM_011544132.1:c.767C>T	XP_011542434.1:p.Ala256Val
XM_011544132.2:c.767C>T	XP_011542434.1:p.Ala256Val
NM_000143.4:c.995C>T MANE Select	NP_000134.2:p.Ala332Val