Canonical Allele Identifier: CA424075805

Gene: FH

Linked Data

• ClinVar Variation Id: 1768757
• ClinVar RCV Id: RCV002382974
• MyVariant Identifiers: chr1:g.241667454G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504154G>C , CM000663.2:g.241504154G>C	GRCh38
NC_000001.10:g.241667454G>C , CM000663.1:g.241667454G>C	GRCh37
NC_000001.9:g.239734077G>C	NCBI36
NG_012338.1:g.20601C>G , LRG_504:g.20601C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1499C>G
ENST00000682162.1:c.1025C>G	ENSP00000508203.1:n.1025C>G
ENST00000682567.1:n.1073C>G
ENST00000683521.1:c.996C>G	ENSP00000506864.1:p.Ala332=
ENST00000684161.1:n.2211C>G
ENST00000684483.1:c.*392C>G	ENSP00000507894.1:n.*392C>G
ENST00000366560.4:c.996C>G MANE Select	ENSP00000355518.4:p.Ala332=
ENST00000366560.3:c.996C>G	ENSP00000355518.3:p.Ala332=
NM_000143.3:c.996C>G , LRG_504t1:c.996C>G	NP_000134.2:p.Ala332=
XM_011544132.1:c.768C>G	XP_011542434.1:p.Ala256=
XM_011544132.2:c.768C>G	XP_011542434.1:p.Ala256=
NM_000143.4:c.996C>G MANE Select	NP_000134.2:p.Ala332=