Canonical Allele Identifier: CA1229580784

Gene: FH

Linked Data

• dbSNP Id: rs1660005231

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508956C>G , CM000663.2:g.241508956C>G	GRCh38
NC_000001.10:g.241672256C>G , CM000663.1:g.241672256C>G	GRCh37
NC_000001.9:g.239738879C>G	NCBI36
NG_012338.1:g.15799G>C , LRG_504:g.15799G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1059-171G>C
ENST00000682162.1:c.585-171G>C	ENSP00000508203.1:n.585-171G>C
ENST00000682567.1:n.633-171G>C
ENST00000683521.1:c.556-171G>C	ENSP00000506864.1:n.556-171G>C
ENST00000684161.1:n.1600G>C
ENST00000684483.1:c.556-196G>C	ENSP00000507894.1:n.556-196G>C
ENST00000366560.4:c.556-171G>C MANE Select	ENSP00000355518.4:n.556-171G>C
ENST00000366560.3:c.556-171G>C	ENSP00000355518.3:n.556-171G>C
NM_000143.3:c.556-171G>C , LRG_504t1:c.556-171G>C	NP_000134.2:n.556-171G>C
XM_011544132.1:c.328-171G>C	XP_011542434.1:n.328-171G>C
XM_011544132.2:c.328-171G>C	XP_011542434.1:n.328-171G>C
NM_000143.4:c.556-171G>C MANE Select	NP_000134.2:n.556-171G>C