Canonical Allele Identifier: CA10581784

Gene: FH

Linked Data

• ClinVar Variation Id: 237116
• ClinVar RCV Id: RCV001023046 ; RCV001782719
• dbSNP Id: rs878853694
• gnomAD v4: 1-241512044-T-C
• MyVariant Identifiers: chr1:g.241675344T>C (hg19) ; chr1:g.241512044T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512044T>C , CM000663.2:g.241512044T>C	GRCh38
NC_000001.10:g.241675344T>C , CM000663.1:g.241675344T>C	GRCh37
NC_000001.9:g.239741967T>C	NCBI36
NG_012338.1:g.12711A>G , LRG_504:g.12711A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.981A>G
ENST00000682162.1:c.507A>G	ENSP00000508203.1:n.507A>G
ENST00000682567.1:n.555A>G
ENST00000683521.1:c.478A>G	ENSP00000506864.1:p.Arg160Gly
ENST00000684483.1:c.478A>G	ENSP00000507894.1:p.Arg160Gly
ENST00000366560.4:c.478A>G MANE Select	ENSP00000355518.4:p.Arg160Gly
ENST00000366560.3:c.478A>G	ENSP00000355518.3:p.Arg160Gly
ENST00000497042.1:n.174A>G
NM_000143.3:c.478A>G , LRG_504t1:c.478A>G	NP_000134.2:p.Arg160Gly
XM_011544132.1:c.250A>G	XP_011542434.1:p.Arg84Gly
XM_011544132.2:c.250A>G	XP_011542434.1:p.Arg84Gly
NM_000143.4:c.478A>G MANE Select	NP_000134.2:p.Arg160Gly