Canonical Allele Identifier: CA1229578753

Gene: FH

Linked Data

• dbSNP Id: rs1659846935
• gnomAD v4: 1-241503972-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241503972T>C , CM000663.2:g.241503972T>C	GRCh38
NC_000001.10:g.241667272T>C , CM000663.1:g.241667272T>C	GRCh37
NC_000001.9:g.239733895T>C	NCBI36
NG_012338.1:g.20783A>G , LRG_504:g.20783A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1611+70A>G
ENST00000682162.1:c.1137+70A>G	ENSP00000508203.1:n.1137+70A>G
ENST00000682567.1:n.1255A>G
ENST00000683521.1:c.1108+70A>G	ENSP00000506864.1:n.1108+70A>G
ENST00000684161.1:n.2323+70A>G
ENST00000684483.1:c.*504+70A>G	ENSP00000507894.1:n.*504+70A>G
ENST00000366560.4:c.1108+70A>G MANE Select	ENSP00000355518.4:n.1108+70A>G
ENST00000366560.3:c.1108+70A>G	ENSP00000355518.3:n.1108+70A>G
NM_000143.3:c.1108+70A>G , LRG_504t1:c.1108+70A>G	NP_000134.2:n.1108+70A>G
XM_011544132.1:c.880+70A>G	XP_011542434.1:n.880+70A>G
XM_011544132.2:c.880+70A>G	XP_011542434.1:n.880+70A>G
NM_000143.4:c.1108+70A>G MANE Select	NP_000134.2:n.1108+70A>G