Canonical Allele Identifier: CA345437324

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241665772A>C (hg19) ; chr1:g.241502472A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502472A>C , CM000663.2:g.241502472A>C	GRCh38
NC_000001.10:g.241665772A>C , CM000663.1:g.241665772A>C	GRCh37
NC_000001.9:g.239732395A>C	NCBI36
NG_012338.1:g.22283T>G , LRG_504:g.22283T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000493477.2:n.1710T>G
ENST00000682162.1:c.1236T>G	ENSP00000508203.1:n.1236T>G
ENST00000682567.1:n.2755T>G
ENST00000683521.1:c.1207T>G	ENSP00000506864.1:p.Phe403Val
ENST00000684161.1:n.2422T>G
ENST00000684483.1:c.*603T>G	ENSP00000507894.1:n.*603T>G
ENST00000366560.4:c.1207T>G MANE Select	ENSP00000355518.4:p.Phe403Val
ENST00000366560.3:c.1207T>G	ENSP00000355518.3:p.Phe403Val
NM_000143.3:c.1207T>G , LRG_504t1:c.1207T>G	NP_000134.2:p.Phe403Val
XM_011544132.1:c.979T>G	XP_011542434.1:p.Phe327Val
XM_011544132.2:c.979T>G	XP_011542434.1:p.Phe327Val
NM_000143.4:c.1207T>G MANE Select	NP_000134.2:p.Phe403Val