Canonical Allele Identifier: CA345439914

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241675299C>T (hg19) ; chr1:g.241511999C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241511999C>T , CM000663.2:g.241511999C>T	GRCh38
NC_000001.10:g.241675299C>T , CM000663.1:g.241675299C>T	GRCh37
NC_000001.9:g.239741922C>T	NCBI36
NG_012338.1:g.12756G>A , LRG_504:g.12756G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1026G>A
ENST00000682162.1:c.552G>A	ENSP00000508203.1:n.552G>A
ENST00000682567.1:n.600G>A
ENST00000683521.1:c.523G>A	ENSP00000506864.1:p.Val175Met
ENST00000684483.1:c.523G>A	ENSP00000507894.1:p.Val175Met
ENST00000366560.4:c.523G>A MANE Select	ENSP00000355518.4:p.Val175Met
ENST00000366560.3:c.523G>A	ENSP00000355518.3:p.Val175Met
ENST00000497042.1:n.219G>A
NM_000143.3:c.523G>A , LRG_504t1:c.523G>A	NP_000134.2:p.Val175Met
XM_011544132.1:c.295G>A	XP_011542434.1:p.Val99Met
XM_011544132.2:c.295G>A	XP_011542434.1:p.Val99Met
NM_000143.4:c.523G>A MANE Select	NP_000134.2:p.Val175Met