Canonical Allele Identifier: CA2651254499

Gene: FH

Linked Data

• gnomAD v4: 1-241500411-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241500411G>T , CM000663.2:g.241500411G>T	GRCh38
NC_000001.10:g.241663711G>T , CM000663.1:g.241663711G>T	GRCh37
NC_000001.9:g.239730334G>T	NCBI36
NG_012338.1:g.24344C>A , LRG_504:g.24344C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1893+26C>A
ENST00000682162.1:c.1419+26C>A	ENSP00000508203.1:n.1419+26C>A
ENST00000682567.1:n.4790+26C>A
ENST00000683521.1:c.1416C>A	ENSP00000506864.1:p.Ile472=
ENST00000684161.1:n.2605+26C>A
ENST00000684483.1:c.*786+26C>A	ENSP00000507894.1:n.*786+26C>A
ENST00000366560.4:c.1390+26C>A MANE Select	ENSP00000355518.4:n.1390+26C>A
ENST00000366560.3:c.1390+26C>A	ENSP00000355518.3:n.1390+26C>A
NM_000143.3:c.1390+26C>A , LRG_504t1:c.1390+26C>A	NP_000134.2:n.1390+26C>A
XM_011544132.1:c.1162+26C>A	XP_011542434.1:n.1162+26C>A
XM_011544132.2:c.1162+26C>A	XP_011542434.1:n.1162+26C>A
NM_000143.4:c.1390+26C>A MANE Select	NP_000134.2:n.1390+26C>A