Canonical Allele Identifier: CA345440043

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241675357T>G (hg19) ; chr1:g.241512057T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512057T>G , CM000663.2:g.241512057T>G	GRCh38
NC_000001.10:g.241675357T>G , CM000663.1:g.241675357T>G	GRCh37
NC_000001.9:g.239741980T>G	NCBI36
NG_012338.1:g.12698A>C , LRG_504:g.12698A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.968A>C
ENST00000682162.1:c.494A>C	ENSP00000508203.1:n.494A>C
ENST00000682567.1:n.542A>C
ENST00000683521.1:c.465A>C	ENSP00000506864.1:p.Glu155Asp
ENST00000684483.1:c.465A>C	ENSP00000507894.1:p.Glu155Asp
ENST00000366560.4:c.465A>C MANE Select	ENSP00000355518.4:p.Glu155Asp
ENST00000366560.3:c.465A>C	ENSP00000355518.3:p.Glu155Asp
ENST00000497042.1:n.161A>C
NM_000143.3:c.465A>C , LRG_504t1:c.465A>C	NP_000134.2:p.Glu155Asp
XM_011544132.1:c.237A>C	XP_011542434.1:p.Glu79Asp
XM_011544132.2:c.237A>C	XP_011542434.1:p.Glu79Asp
NM_000143.4:c.465A>C MANE Select	NP_000134.2:p.Glu155Asp