Canonical Allele Identifier: CA1229578088

Gene: FH

Linked Data

• dbSNP Id: rs1659802405
• gnomAD v4: 1-241502384-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502384C>T , CM000663.2:g.241502384C>T	GRCh38
NC_000001.10:g.241665684C>T , CM000663.1:g.241665684C>T	GRCh37
NC_000001.9:g.239732307C>T	NCBI36
NG_012338.1:g.22371G>A , LRG_504:g.22371G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1739+59G>A
ENST00000682162.1:c.1265+59G>A	ENSP00000508203.1:n.1265+59G>A
ENST00000682567.1:n.2843G>A
ENST00000683521.1:c.1236+59G>A	ENSP00000506864.1:n.1236+59G>A
ENST00000684161.1:n.2451+59G>A
ENST00000684483.1:c.*632+59G>A	ENSP00000507894.1:n.*632+59G>A
ENST00000366560.4:c.1236+59G>A MANE Select	ENSP00000355518.4:n.1236+59G>A
ENST00000366560.3:c.1236+59G>A	ENSP00000355518.3:n.1236+59G>A
NM_000143.3:c.1236+59G>A , LRG_504t1:c.1236+59G>A	NP_000134.2:n.1236+59G>A
XM_011544132.1:c.1008+59G>A	XP_011542434.1:n.1008+59G>A
XM_011544132.2:c.1008+59G>A	XP_011542434.1:n.1008+59G>A
NM_000143.4:c.1236+59G>A MANE Select	NP_000134.2:n.1236+59G>A