Canonical Allele Identifier: CA1229582155

Gene: FH

Linked Data

• dbSNP Id: rs1660107858
• gnomAD v3: 1-241512274-T-TA
• gnomAD v4: 1-241512274-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512279dup , CM000663.2:g.241512279dup	GRCh38
NC_000001.10:g.241675579dup , CM000663.1:g.241675579dup	GRCh37
NC_000001.9:g.239742202dup	NCBI36
NG_012338.1:g.12480dup , LRG_504:g.12480dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.882-132dup
ENST00000682162.1:c.408-132dup	ENSP00000508203.1:n.408-132dup
ENST00000682567.1:n.456-132dup
ENST00000683521.1:c.379-132dup	ENSP00000506864.1:n.379-132dup
ENST00000684483.1:c.379-132dup	ENSP00000507894.1:n.379-132dup
ENST00000366560.4:c.379-132dup MANE Select	ENSP00000355518.4:n.379-132dup
ENST00000366560.3:c.379-132dup	ENSP00000355518.3:n.379-132dup
ENST00000497042.1:n.75-132dup
NM_000143.3:c.379-132dup , LRG_504t1:c.379-132dup	NP_000134.2:n.379-132dup
XM_011544132.1:c.151-132dup	XP_011542434.1:n.151-132dup
XM_011544132.2:c.151-132dup	XP_011542434.1:n.151-132dup
NM_000143.4:c.379-132dup MANE Select	NP_000134.2:n.379-132dup