Canonical Allele Identifier: CA345439238

Gene: FH

Linked Data

• ClinVar Variation Id: 1072934
• ClinVar RCV Id: RCV002551543
• dbSNP Id: rs863223967
• MyVariant Identifiers: chr1:g.241671953T>G (hg19) ; chr1:g.241508653T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508653T>G , CM000663.2:g.241508653T>G	GRCh38
NC_000001.10:g.241671953T>G , CM000663.1:g.241671953T>G	GRCh37
NC_000001.9:g.239738576T>G	NCBI36
NG_012338.1:g.16102A>C , LRG_504:g.16102A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000493477.2:n.1191A>C
ENST00000682162.1:c.717A>C	ENSP00000508203.1:n.717A>C
ENST00000682567.1:n.765A>C
ENST00000683521.1:c.688A>C	ENSP00000506864.1:p.Lys230Gln
ENST00000684161.1:n.1903A>C
ENST00000684483.1:c.*84A>C	ENSP00000507894.1:n.*84A>C
ENST00000366560.4:c.688A>C MANE Select	ENSP00000355518.4:p.Lys230Gln
ENST00000366560.3:c.688A>C	ENSP00000355518.3:p.Lys230Gln
NM_000143.3:c.688A>C , LRG_504t1:c.688A>C	NP_000134.2:p.Lys230Gln
XM_011544132.1:c.460A>C	XP_011542434.1:p.Lys154Gln
XM_011544132.2:c.460A>C	XP_011542434.1:p.Lys154Gln
NM_000143.4:c.688A>C MANE Select	NP_000134.2:p.Lys230Gln