Canonical Allele Identifier: CA2651255184

Gene: FH

Linked Data

• gnomAD v4: 1-241504001-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504001A>T , CM000663.2:g.241504001A>T	GRCh38
NC_000001.10:g.241667301A>T , CM000663.1:g.241667301A>T	GRCh37
NC_000001.9:g.239733924A>T	NCBI36
NG_012338.1:g.20754T>A , LRG_504:g.20754T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1611+41T>A
ENST00000682162.1:c.1137+41T>A	ENSP00000508203.1:n.1137+41T>A
ENST00000682567.1:n.1226T>A
ENST00000683521.1:c.1108+41T>A	ENSP00000506864.1:n.1108+41T>A
ENST00000684161.1:n.2323+41T>A
ENST00000684483.1:c.*504+41T>A	ENSP00000507894.1:n.*504+41T>A
ENST00000366560.4:c.1108+41T>A MANE Select	ENSP00000355518.4:n.1108+41T>A
ENST00000366560.3:c.1108+41T>A	ENSP00000355518.3:n.1108+41T>A
NM_000143.3:c.1108+41T>A , LRG_504t1:c.1108+41T>A	NP_000134.2:n.1108+41T>A
XM_011544132.1:c.880+41T>A	XP_011542434.1:n.880+41T>A
XM_011544132.2:c.880+41T>A	XP_011542434.1:n.880+41T>A
NM_000143.4:c.1108+41T>A MANE Select	NP_000134.2:n.1108+41T>A