Canonical Allele Identifier: CA424076309

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241675363T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512063T>G , CM000663.2:g.241512063T>G	GRCh38
NC_000001.10:g.241675363T>G , CM000663.1:g.241675363T>G	GRCh37
NC_000001.9:g.239741986T>G	NCBI36
NG_012338.1:g.12692A>C , LRG_504:g.12692A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.962A>C
ENST00000682162.1:c.488A>C	ENSP00000508203.1:n.488A>C
ENST00000682567.1:n.536A>C
ENST00000683521.1:c.459A>C	ENSP00000506864.1:p.Val153=
ENST00000684483.1:c.459A>C	ENSP00000507894.1:p.Val153=
ENST00000366560.4:c.459A>C MANE Select	ENSP00000355518.4:p.Val153=
ENST00000366560.3:c.459A>C	ENSP00000355518.3:p.Val153=
ENST00000497042.1:n.155A>C
NM_000143.3:c.459A>C , LRG_504t1:c.459A>C	NP_000134.2:p.Val153=
XM_011544132.1:c.231A>C	XP_011542434.1:p.Val77=
XM_011544132.2:c.231A>C	XP_011542434.1:p.Val77=
NM_000143.4:c.459A>C MANE Select	NP_000134.2:p.Val153=