Canonical Allele Identifier: CA424076033

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241671933A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508633A>T , CM000663.2:g.241508633A>T	GRCh38
NC_000001.10:g.241671933A>T , CM000663.1:g.241671933A>T	GRCh37
NC_000001.9:g.239738556A>T	NCBI36
NG_012338.1:g.16122T>A , LRG_504:g.16122T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1211T>A
ENST00000682162.1:c.737T>A	ENSP00000508203.1:n.737T>A
ENST00000682567.1:n.785T>A
ENST00000683521.1:c.708T>A	ENSP00000506864.1:p.Thr236=
ENST00000684161.1:n.1923T>A
ENST00000684483.1:c.*104T>A	ENSP00000507894.1:n.*104T>A
ENST00000366560.4:c.708T>A MANE Select	ENSP00000355518.4:p.Thr236=
ENST00000366560.3:c.708T>A	ENSP00000355518.3:p.Thr236=
NM_000143.3:c.708T>A , LRG_504t1:c.708T>A	NP_000134.2:p.Thr236=
XM_011544132.1:c.480T>A	XP_011542434.1:p.Thr160=
XM_011544132.2:c.480T>A	XP_011542434.1:p.Thr160=
NM_000143.4:c.708T>A MANE Select	NP_000134.2:p.Thr236=