Canonical Allele Identifier: CA345439210

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241671937T>A (hg19) ; chr1:g.241508637T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508637T>A , CM000663.2:g.241508637T>A	GRCh38
NC_000001.10:g.241671937T>A , CM000663.1:g.241671937T>A	GRCh37
NC_000001.9:g.239738560T>A	NCBI36
NG_012338.1:g.16118A>T , LRG_504:g.16118A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000493477.2:n.1207A>T
ENST00000682162.1:c.733A>T	ENSP00000508203.1:n.733A>T
ENST00000682567.1:n.781A>T
ENST00000683521.1:c.704A>T	ENSP00000506864.1:p.His235Leu
ENST00000684161.1:n.1919A>T
ENST00000684483.1:c.*100A>T	ENSP00000507894.1:n.*100A>T
ENST00000366560.4:c.704A>T MANE Select	ENSP00000355518.4:p.His235Leu
ENST00000366560.3:c.704A>T	ENSP00000355518.3:p.His235Leu
NM_000143.3:c.704A>T , LRG_504t1:c.704A>T	NP_000134.2:p.His235Leu
XM_011544132.1:c.476A>T	XP_011542434.1:p.His159Leu
XM_011544132.2:c.476A>T	XP_011542434.1:p.His159Leu
NM_000143.4:c.704A>T MANE Select	NP_000134.2:p.His235Leu