Canonical Allele Identifier: CA16610104

Gene: FH

Linked Data

• ClinVar Variation Id: 405925
• ClinVar RCV Id: RCV002525542
• dbSNP Id: rs1060499639
• MyVariant Identifiers: chr1:g.241669384C>T (hg19) ; chr1:g.241506084C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241506084C>T , CM000663.2:g.241506084C>T	GRCh38
NC_000001.10:g.241669384C>T , CM000663.1:g.241669384C>T	GRCh37
NC_000001.9:g.239736007C>T	NCBI36
NG_012338.1:g.18671G>A , LRG_504:g.18671G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1326G>A
ENST00000682162.1:c.852G>A	ENSP00000508203.1:n.852G>A
ENST00000682567.1:n.900G>A
ENST00000683521.1:c.823G>A	ENSP00000506864.1:p.Gly275Arg
ENST00000684161.1:n.2038G>A
ENST00000684483.1:c.*219G>A	ENSP00000507894.1:n.*219G>A
ENST00000366560.4:c.823G>A MANE Select	ENSP00000355518.4:p.Gly275Arg
ENST00000366560.3:c.823G>A	ENSP00000355518.3:p.Gly275Arg
NM_000143.3:c.823G>A , LRG_504t1:c.823G>A	NP_000134.2:p.Gly275Arg
XM_011544132.1:c.595G>A	XP_011542434.1:p.Gly199Arg
XM_011544132.2:c.595G>A	XP_011542434.1:p.Gly199Arg
NM_000143.4:c.823G>A MANE Select	NP_000134.2:p.Gly275Arg