Canonical Allele Identifier: CA16610040

Gene: FH

Linked Data

• ClinVar Variation Id: 413611
• ClinVar RCV Id: RCV002526472 ; RCV002374833
• dbSNP Id: rs1060504078
• gnomAD v4: 1-241504169-G-A
• MyVariant Identifiers: chr1:g.241667469G>A (hg19) ; chr1:g.241504169G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504169G>A , CM000663.2:g.241504169G>A	GRCh38
NC_000001.10:g.241667469G>A , CM000663.1:g.241667469G>A	GRCh37
NC_000001.9:g.239734092G>A	NCBI36
NG_012338.1:g.20586C>T , LRG_504:g.20586C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1484C>T
ENST00000682162.1:c.1010C>T	ENSP00000508203.1:n.1010C>T
ENST00000682567.1:n.1058C>T
ENST00000683521.1:c.981C>T	ENSP00000506864.1:p.Ala327=
ENST00000684161.1:n.2196C>T
ENST00000684483.1:c.*377C>T	ENSP00000507894.1:n.*377C>T
ENST00000366560.4:c.981C>T MANE Select	ENSP00000355518.4:p.Ala327=
ENST00000366560.3:c.981C>T	ENSP00000355518.3:p.Ala327=
NM_000143.3:c.981C>T , LRG_504t1:c.981C>T	NP_000134.2:p.Ala327=
XM_011544132.1:c.753C>T	XP_011542434.1:p.Ala251=
XM_011544132.2:c.753C>T	XP_011542434.1:p.Ala251=
NM_000143.4:c.981C>T MANE Select	NP_000134.2:p.Ala327=