Canonical Allele Identifier: CA16609381

Gene: FH

Linked Data

• ClinVar Variation Id: 393556
• ClinVar RCV Id: RCV000445628
• dbSNP Id: rs1060499627
• gnomAD v4: 1-241519586-C-A
• MyVariant Identifiers: chr1:g.241682886C>A (hg19) ; chr1:g.241519586C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241519586C>A , CM000663.2:g.241519586C>A	GRCh38
NC_000001.10:g.241682886C>A , CM000663.1:g.241682886C>A	GRCh37
NC_000001.9:g.239749509C>A	NCBI36
NG_012338.1:g.5169G>T , LRG_504:g.5169G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.109G>T
ENST00000682162.1:c.132+5G>T	ENSP00000508203.1:n.132+5G>T
ENST00000682567.1:n.209+5G>T
ENST00000683521.1:c.132+5G>T	ENSP00000506864.1:n.132+5G>T
ENST00000684483.1:c.132+5G>T	ENSP00000507894.1:n.132+5G>T
ENST00000366560.4:c.132+5G>T MANE Select	ENSP00000355518.4:n.132+5G>T
ENST00000366560.3:c.132+5G>T	ENSP00000355518.3:n.132+5G>T
NM_000143.3:c.132+5G>T , LRG_504t1:c.132+5G>T	NP_000134.2:n.132+5G>T
XM_011544132.2:c.-623G>T	XP_011542434.1:n.-623G>T
NM_000143.4:c.132+5G>T MANE Select	NP_000134.2:n.132+5G>T