Canonical Allele Identifier: CA345440226

Gene: FH

Linked Data

• dbSNP Id: rs2147922034
• MyVariant Identifiers: chr1:g.241675439G>T (hg19) ; chr1:g.241512139G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512139G>T , CM000663.2:g.241512139G>T	GRCh38
NC_000001.10:g.241675439G>T , CM000663.1:g.241675439G>T	GRCh37
NC_000001.9:g.239742062G>T	NCBI36
NG_012338.1:g.12616C>A , LRG_504:g.12616C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.886C>A
ENST00000682162.1:c.412C>A	ENSP00000508203.1:n.412C>A
ENST00000682567.1:n.460C>A
ENST00000683521.1:c.383C>A	ENSP00000506864.1:p.Ala128Asp
ENST00000684483.1:c.383C>A	ENSP00000507894.1:p.Ala128Asp
ENST00000366560.4:c.383C>A MANE Select	ENSP00000355518.4:p.Ala128Asp
ENST00000366560.3:c.383C>A	ENSP00000355518.3:p.Ala128Asp
ENST00000497042.1:n.79C>A
NM_000143.3:c.383C>A , LRG_504t1:c.383C>A	NP_000134.2:p.Ala128Asp
XM_011544132.1:c.155C>A	XP_011542434.1:p.Ala52Asp
XM_011544132.2:c.155C>A	XP_011542434.1:p.Ala52Asp
NM_000143.4:c.383C>A MANE Select	NP_000134.2:p.Ala128Asp