Canonical Allele Identifier: CA424076315

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241675381A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512081A>G , CM000663.2:g.241512081A>G	GRCh38
NC_000001.10:g.241675381A>G , CM000663.1:g.241675381A>G	GRCh37
NC_000001.9:g.239742004A>G	NCBI36
NG_012338.1:g.12674T>C , LRG_504:g.12674T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.944T>C
ENST00000682162.1:c.470T>C	ENSP00000508203.1:n.470T>C
ENST00000682567.1:n.518T>C
ENST00000683521.1:c.441T>C	ENSP00000506864.1:p.Thr147=
ENST00000684483.1:c.441T>C	ENSP00000507894.1:p.Thr147=
ENST00000366560.4:c.441T>C MANE Select	ENSP00000355518.4:p.Thr147=
ENST00000366560.3:c.441T>C	ENSP00000355518.3:p.Thr147=
ENST00000497042.1:n.137T>C
NM_000143.3:c.441T>C , LRG_504t1:c.441T>C	NP_000134.2:p.Thr147=
XM_011544132.1:c.213T>C	XP_011542434.1:p.Thr71=
XM_011544132.2:c.213T>C	XP_011542434.1:p.Thr71=
NM_000143.4:c.441T>C MANE Select	NP_000134.2:p.Thr147=