Canonical Allele Identifier: CA424075732

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241667349G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504049G>T , CM000663.2:g.241504049G>T	GRCh38
NC_000001.10:g.241667349G>T , CM000663.1:g.241667349G>T	GRCh37
NC_000001.9:g.239733972G>T	NCBI36
NG_012338.1:g.20706C>A , LRG_504:g.20706C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1604C>A
ENST00000682162.1:c.1130C>A	ENSP00000508203.1:n.1130C>A
ENST00000682567.1:n.1178C>A
ENST00000683521.1:c.1101C>A	ENSP00000506864.1:p.Ile367=
ENST00000684161.1:n.2316C>A
ENST00000684483.1:c.*497C>A	ENSP00000507894.1:n.*497C>A
ENST00000366560.4:c.1101C>A MANE Select	ENSP00000355518.4:p.Ile367=
ENST00000366560.3:c.1101C>A	ENSP00000355518.3:p.Ile367=
NM_000143.3:c.1101C>A , LRG_504t1:c.1101C>A	NP_000134.2:p.Ile367=
XM_011544132.1:c.873C>A	XP_011542434.1:p.Ile291=
XM_011544132.2:c.873C>A	XP_011542434.1:p.Ile291=
NM_000143.4:c.1101C>A MANE Select	NP_000134.2:p.Ile367=