Canonical Allele Identifier: CA345438332

Gene: FH

Linked Data

• ClinVar Variation Id: 2754594
• ClinVar RCV Id: RCV003563942
• dbSNP Id: rs766441385
• MyVariant Identifiers: chr1:g.241667492C>G (hg19) ; chr1:g.241504192C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504192C>G , CM000663.2:g.241504192C>G	GRCh38
NC_000001.10:g.241667492C>G , CM000663.1:g.241667492C>G	GRCh37
NC_000001.9:g.239734115C>G	NCBI36
NG_012338.1:g.20563G>C , LRG_504:g.20563G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1461G>C
ENST00000682162.1:c.987G>C	ENSP00000508203.1:n.987G>C
ENST00000682567.1:n.1035G>C
ENST00000683521.1:c.958G>C	ENSP00000506864.1:p.Ala320Pro
ENST00000684161.1:n.2173G>C
ENST00000684483.1:c.*354G>C	ENSP00000507894.1:n.*354G>C
ENST00000366560.4:c.958G>C MANE Select	ENSP00000355518.4:p.Ala320Pro
ENST00000366560.3:c.958G>C	ENSP00000355518.3:p.Ala320Pro
NM_000143.3:c.958G>C , LRG_504t1:c.958G>C	NP_000134.2:p.Ala320Pro
XM_011544132.1:c.730G>C	XP_011542434.1:p.Ala244Pro
XM_011544132.2:c.730G>C	XP_011542434.1:p.Ala244Pro
NM_000143.4:c.958G>C MANE Select	NP_000134.2:p.Ala320Pro