Canonical Allele Identifier: CA1229584081

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241517181C= , CM000663.2:g.241517181C=	GRCh38
NC_000001.10:g.241680481C= , CM000663.1:g.241680481C=	GRCh37
NC_000001.9:g.239747104C=	NCBI36
NG_012338.1:g.7574G= , LRG_504:g.7574G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000143.4:c.267+1G= MANE Select	NP_000134.2:n.267+1G=
ENST00000366560.4:c.267+1G= MANE Select	ENSP00000355518.4:n.267+1G=
NM_000143.3:c.267+1G= , LRG_504t1:c.267+1G=	NP_000134.2:n.267+1G=
ENST00000366560.3:c.267+1G=	ENSP00000355518.3:n.267+1G=
ENST00000493477.1:n.380+1G=
ENST00000493477.2:n.770+1G=
ENST00000682162.1:c.296+1G=	ENSP00000508203.1:n.296+1G=
ENST00000682567.1:n.344+1G=
ENST00000683521.1:c.267+1G=	ENSP00000506864.1:n.267+1G=
ENST00000684483.1:c.267+1G=	ENSP00000507894.1:n.267+1G=
XM_011544132.1:c.39+1G=	XP_011542434.1:n.39+1G=
XM_011544132.2:c.39+1G=	XP_011542434.1:n.39+1G=