Canonical Allele Identifier: CA345438339

Gene: FH

Linked Data

• ClinVar Variation Id: 2203013
• ClinVar RCV Id: RCV002634357
• gnomAD v4: 1-241504195-C-T
• MyVariant Identifiers: chr1:g.241667495C>T (hg19) ; chr1:g.241504195C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504195C>T , CM000663.2:g.241504195C>T	GRCh38
NC_000001.10:g.241667495C>T , CM000663.1:g.241667495C>T	GRCh37
NC_000001.9:g.239734118C>T	NCBI36
NG_012338.1:g.20560G>A , LRG_504:g.20560G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1458G>A
ENST00000682162.1:c.984G>A	ENSP00000508203.1:n.984G>A
ENST00000682567.1:n.1032G>A
ENST00000683521.1:c.955G>A	ENSP00000506864.1:p.Asp319Asn
ENST00000684161.1:n.2170G>A
ENST00000684483.1:c.*351G>A	ENSP00000507894.1:n.*351G>A
ENST00000366560.4:c.955G>A MANE Select	ENSP00000355518.4:p.Asp319Asn
ENST00000366560.3:c.955G>A	ENSP00000355518.3:p.Asp319Asn
NM_000143.3:c.955G>A , LRG_504t1:c.955G>A	NP_000134.2:p.Asp319Asn
XM_011544132.1:c.727G>A	XP_011542434.1:p.Asp243Asn
XM_011544132.2:c.727G>A	XP_011542434.1:p.Asp243Asn
NM_000143.4:c.955G>A MANE Select	NP_000134.2:p.Asp319Asn