Canonical Allele Identifier: CA424076617

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241680593T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241517293T>A , CM000663.2:g.241517293T>A	GRCh38
NC_000001.10:g.241680593T>A , CM000663.1:g.241680593T>A	GRCh37
NC_000001.9:g.239747216T>A	NCBI36
NG_012338.1:g.7462A>T , LRG_504:g.7462A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.659A>T
ENST00000682162.1:c.185A>T	ENSP00000508203.1:p.Ter62Leu
ENST00000682567.1:n.233A>T
ENST00000683521.1:c.156A>T	ENSP00000506864.1:p.Ile52=
ENST00000684483.1:c.156A>T	ENSP00000507894.1:p.Ile52=
ENST00000366560.4:c.156A>T MANE Select	ENSP00000355518.4:p.Ile52=
ENST00000366560.3:c.156A>T	ENSP00000355518.3:p.Ile52=
ENST00000493477.1:n.269A>T
NM_000143.3:c.156A>T , LRG_504t1:c.156A>T	NP_000134.2:p.Ile52=
XM_011544132.1:c.-73A>T	XP_011542434.1:n.-73A>T
XM_011544132.2:c.-73A>T	XP_011542434.1:n.-73A>T
NM_000143.4:c.156A>T MANE Select	NP_000134.2:p.Ile52=