Canonical Allele Identifier: CA345437312

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241665769C>G (hg19) ; chr1:g.241502469C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502469C>G , CM000663.2:g.241502469C>G	GRCh38
NC_000001.10:g.241665769C>G , CM000663.1:g.241665769C>G	GRCh37
NC_000001.9:g.239732392C>G	NCBI36
NG_012338.1:g.22286G>C , LRG_504:g.22286G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1713G>C
ENST00000682162.1:c.1239G>C	ENSP00000508203.1:n.1239G>C
ENST00000682567.1:n.2758G>C
ENST00000683521.1:c.1210G>C	ENSP00000506864.1:p.Glu404Gln
ENST00000684161.1:n.2425G>C
ENST00000684483.1:c.*606G>C	ENSP00000507894.1:n.*606G>C
ENST00000366560.4:c.1210G>C MANE Select	ENSP00000355518.4:p.Glu404Gln
ENST00000366560.3:c.1210G>C	ENSP00000355518.3:p.Glu404Gln
NM_000143.3:c.1210G>C , LRG_504t1:c.1210G>C	NP_000134.2:p.Glu404Gln
XM_011544132.1:c.982G>C	XP_011542434.1:p.Glu328Gln
XM_011544132.2:c.982G>C	XP_011542434.1:p.Glu328Gln
NM_000143.4:c.1210G>C MANE Select	NP_000134.2:p.Glu404Gln