Canonical Allele Identifier: CA345439319

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241671994T>C (hg19) ; chr1:g.241508694T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508694T>C , CM000663.2:g.241508694T>C	GRCh38
NC_000001.10:g.241671994T>C , CM000663.1:g.241671994T>C	GRCh37
NC_000001.9:g.239738617T>C	NCBI36
NG_012338.1:g.16061A>G , LRG_504:g.16061A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1150A>G
ENST00000682162.1:c.676A>G	ENSP00000508203.1:n.676A>G
ENST00000682567.1:n.724A>G
ENST00000683521.1:c.647A>G	ENSP00000506864.1:p.Asp216Gly
ENST00000684161.1:n.1862A>G
ENST00000684483.1:c.*43A>G	ENSP00000507894.1:n.*43A>G
ENST00000366560.4:c.647A>G MANE Select	ENSP00000355518.4:p.Asp216Gly
ENST00000366560.3:c.647A>G	ENSP00000355518.3:p.Asp216Gly
NM_000143.3:c.647A>G , LRG_504t1:c.647A>G	NP_000134.2:p.Asp216Gly
XM_011544132.1:c.419A>G	XP_011542434.1:p.Asp140Gly
XM_011544132.2:c.419A>G	XP_011542434.1:p.Asp140Gly
NM_000143.4:c.647A>G MANE Select	NP_000134.2:p.Asp216Gly