Canonical Allele Identifier: CA345438195

Gene: FH

Linked Data

• dbSNP Id: rs121913122
• MyVariant Identifiers: chr1:g.241667423G>C (hg19) ; chr1:g.241504123G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504123G>C , CM000663.2:g.241504123G>C	GRCh38
NC_000001.10:g.241667423G>C , CM000663.1:g.241667423G>C	GRCh37
NC_000001.9:g.239734046G>C	NCBI36
NG_012338.1:g.20632C>G , LRG_504:g.20632C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1530C>G
ENST00000682162.1:c.1056C>G	ENSP00000508203.1:n.1056C>G
ENST00000682567.1:n.1104C>G
ENST00000683521.1:c.1027C>G	ENSP00000506864.1:p.Arg343Gly
ENST00000684161.1:n.2242C>G
ENST00000684483.1:c.*423C>G	ENSP00000507894.1:n.*423C>G
ENST00000366560.4:c.1027C>G MANE Select	ENSP00000355518.4:p.Arg343Gly
ENST00000366560.3:c.1027C>G	ENSP00000355518.3:p.Arg343Gly
NM_000143.3:c.1027C>G , LRG_504t1:c.1027C>G	NP_000134.2:p.Arg343Gly
XM_011544132.1:c.799C>G	XP_011542434.1:p.Arg267Gly
XM_011544132.2:c.799C>G	XP_011542434.1:p.Arg267Gly
NM_000143.4:c.1027C>G MANE Select	NP_000134.2:p.Arg343Gly