Canonical Allele Identifier: CA345439152

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241671908C>G (hg19) ; chr1:g.241508608C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508608C>G , CM000663.2:g.241508608C>G	GRCh38
NC_000001.10:g.241671908C>G , CM000663.1:g.241671908C>G	GRCh37
NC_000001.9:g.239738531C>G	NCBI36
NG_012338.1:g.16147G>C , LRG_504:g.16147G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000493477.2:n.1236G>C
ENST00000682162.1:c.762G>C	ENSP00000508203.1:n.762G>C
ENST00000682567.1:n.810G>C
ENST00000683521.1:c.733G>C	ENSP00000506864.1:p.Gly245Arg
ENST00000684161.1:n.1948G>C
ENST00000684483.1:c.*129G>C	ENSP00000507894.1:n.*129G>C
ENST00000366560.4:c.733G>C MANE Select	ENSP00000355518.4:p.Gly245Arg
ENST00000366560.3:c.733G>C	ENSP00000355518.3:p.Gly245Arg
NM_000143.3:c.733G>C , LRG_504t1:c.733G>C	NP_000134.2:p.Gly245Arg
XM_011544132.1:c.505G>C	XP_011542434.1:p.Gly169Arg
XM_011544132.2:c.505G>C	XP_011542434.1:p.Gly169Arg
NM_000143.4:c.733G>C MANE Select	NP_000134.2:p.Gly245Arg