Canonical Allele Identifier: CA424076022

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241671918T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508618T>A , CM000663.2:g.241508618T>A	GRCh38
NC_000001.10:g.241671918T>A , CM000663.1:g.241671918T>A	GRCh37
NC_000001.9:g.239738541T>A	NCBI36
NG_012338.1:g.16137A>T , LRG_504:g.16137A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1226A>T
ENST00000682162.1:c.752A>T	ENSP00000508203.1:n.752A>T
ENST00000682567.1:n.800A>T
ENST00000683521.1:c.723A>T	ENSP00000506864.1:p.Pro241=
ENST00000684161.1:n.1938A>T
ENST00000684483.1:c.*119A>T	ENSP00000507894.1:n.*119A>T
ENST00000366560.4:c.723A>T MANE Select	ENSP00000355518.4:p.Pro241=
ENST00000366560.3:c.723A>T	ENSP00000355518.3:p.Pro241=
NM_000143.3:c.723A>T , LRG_504t1:c.723A>T	NP_000134.2:p.Pro241=
XM_011544132.1:c.495A>T	XP_011542434.1:p.Pro165=
XM_011544132.2:c.495A>T	XP_011542434.1:p.Pro165=
NM_000143.4:c.723A>T MANE Select	NP_000134.2:p.Pro241=