Canonical Allele Identifier: CA345437329

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241665773A>T (hg19) ; chr1:g.241502473A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502473A>T , CM000663.2:g.241502473A>T	GRCh38
NC_000001.10:g.241665773A>T , CM000663.1:g.241665773A>T	GRCh37
NC_000001.9:g.239732396A>T	NCBI36
NG_012338.1:g.22282T>A , LRG_504:g.22282T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000493477.2:n.1709T>A
ENST00000682162.1:c.1235T>A	ENSP00000508203.1:n.1235T>A
ENST00000682567.1:n.2754T>A
ENST00000683521.1:c.1206T>A	ENSP00000506864.1:p.His402Gln
ENST00000684161.1:n.2421T>A
ENST00000684483.1:c.*602T>A	ENSP00000507894.1:n.*602T>A
ENST00000366560.4:c.1206T>A MANE Select	ENSP00000355518.4:p.His402Gln
ENST00000366560.3:c.1206T>A	ENSP00000355518.3:p.His402Gln
NM_000143.3:c.1206T>A , LRG_504t1:c.1206T>A	NP_000134.2:p.His402Gln
XM_011544132.1:c.978T>A	XP_011542434.1:p.His326Gln
XM_011544132.2:c.978T>A	XP_011542434.1:p.His326Gln
NM_000143.4:c.1206T>A MANE Select	NP_000134.2:p.His402Gln