Canonical Allele Identifier: CA424075757

Gene: FH

Linked Data

• dbSNP Id: rs2147916101
• MyVariant Identifiers: chr1:g.241667391C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504091C>A , CM000663.2:g.241504091C>A	GRCh38
NC_000001.10:g.241667391C>A , CM000663.1:g.241667391C>A	GRCh37
NC_000001.9:g.239734014C>A	NCBI36
NG_012338.1:g.20664G>T , LRG_504:g.20664G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1562G>T
ENST00000682162.1:c.1088G>T	ENSP00000508203.1:n.1088G>T
ENST00000682567.1:n.1136G>T
ENST00000683521.1:c.1059G>T	ENSP00000506864.1:p.Leu353=
ENST00000684161.1:n.2274G>T
ENST00000684483.1:c.*455G>T	ENSP00000507894.1:n.*455G>T
ENST00000366560.4:c.1059G>T MANE Select	ENSP00000355518.4:p.Leu353=
ENST00000366560.3:c.1059G>T	ENSP00000355518.3:p.Leu353=
NM_000143.3:c.1059G>T , LRG_504t1:c.1059G>T	NP_000134.2:p.Leu353=
XM_011544132.1:c.831G>T	XP_011542434.1:p.Leu277=
XM_011544132.2:c.831G>T	XP_011542434.1:p.Leu277=
NM_000143.4:c.1059G>T MANE Select	NP_000134.2:p.Leu353=