Canonical Allele Identifier: CA345438310

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241667480G>A (hg19) ; chr1:g.241504180G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504180G>A , CM000663.2:g.241504180G>A	GRCh38
NC_000001.10:g.241667480G>A , CM000663.1:g.241667480G>A	GRCh37
NC_000001.9:g.239734103G>A	NCBI36
NG_012338.1:g.20575C>T , LRG_504:g.20575C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1473C>T
ENST00000682162.1:c.999C>T	ENSP00000508203.1:n.999C>T
ENST00000682567.1:n.1047C>T
ENST00000683521.1:c.970C>T	ENSP00000506864.1:p.Leu324Phe
ENST00000684161.1:n.2185C>T
ENST00000684483.1:c.*366C>T	ENSP00000507894.1:n.*366C>T
ENST00000366560.4:c.970C>T MANE Select	ENSP00000355518.4:p.Leu324Phe
ENST00000366560.3:c.970C>T	ENSP00000355518.3:p.Leu324Phe
NM_000143.3:c.970C>T , LRG_504t1:c.970C>T	NP_000134.2:p.Leu324Phe
XM_011544132.1:c.742C>T	XP_011542434.1:p.Leu248Phe
XM_011544132.2:c.742C>T	XP_011542434.1:p.Leu248Phe
NM_000143.4:c.970C>T MANE Select	NP_000134.2:p.Leu324Phe