Canonical Allele Identifier: CA2651254980

Gene: FH

Linked Data

• gnomAD v4: 1-241508831-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508831C>T , CM000663.2:g.241508831C>T	GRCh38
NC_000001.10:g.241672131C>T , CM000663.1:g.241672131C>T	GRCh37
NC_000001.9:g.239738754C>T	NCBI36
NG_012338.1:g.15924G>A , LRG_504:g.15924G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1059-46G>A
ENST00000682162.1:c.585-46G>A	ENSP00000508203.1:n.585-46G>A
ENST00000682567.1:n.633-46G>A
ENST00000683521.1:c.556-46G>A	ENSP00000506864.1:n.556-46G>A
ENST00000684161.1:n.1725G>A
ENST00000684483.1:c.556-71G>A	ENSP00000507894.1:n.556-71G>A
ENST00000366560.4:c.556-46G>A MANE Select	ENSP00000355518.4:n.556-46G>A
ENST00000366560.3:c.556-46G>A	ENSP00000355518.3:n.556-46G>A
NM_000143.3:c.556-46G>A , LRG_504t1:c.556-46G>A	NP_000134.2:n.556-46G>A
XM_011544132.1:c.328-46G>A	XP_011542434.1:n.328-46G>A
XM_011544132.2:c.328-46G>A	XP_011542434.1:n.328-46G>A
NM_000143.4:c.556-46G>A MANE Select	NP_000134.2:n.556-46G>A