Canonical Allele Identifier: CA424076289

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241675324T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512024T>G , CM000663.2:g.241512024T>G	GRCh38
NC_000001.10:g.241675324T>G , CM000663.1:g.241675324T>G	GRCh37
NC_000001.9:g.239741947T>G	NCBI36
NG_012338.1:g.12731A>C , LRG_504:g.12731A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1001A>C
ENST00000682162.1:c.527A>C	ENSP00000508203.1:n.527A>C
ENST00000682567.1:n.575A>C
ENST00000683521.1:c.498A>C	ENSP00000506864.1:p.Gly166=
ENST00000684483.1:c.498A>C	ENSP00000507894.1:p.Gly166=
ENST00000366560.4:c.498A>C MANE Select	ENSP00000355518.4:p.Gly166=
ENST00000366560.3:c.498A>C	ENSP00000355518.3:p.Gly166=
ENST00000497042.1:n.194A>C
NM_000143.3:c.498A>C , LRG_504t1:c.498A>C	NP_000134.2:p.Gly166=
XM_011544132.1:c.270A>C	XP_011542434.1:p.Gly90=
XM_011544132.2:c.270A>C	XP_011542434.1:p.Gly90=
NM_000143.4:c.498A>C MANE Select	NP_000134.2:p.Gly166=