Canonical Allele Identifier: CA345440108

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241675386C>A (hg19) ; chr1:g.241512086C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512086C>A , CM000663.2:g.241512086C>A	GRCh38
NC_000001.10:g.241675386C>A , CM000663.1:g.241675386C>A	GRCh37
NC_000001.9:g.239742009C>A	NCBI36
NG_012338.1:g.12669G>T , LRG_504:g.12669G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.939G>T
ENST00000682162.1:c.465G>T	ENSP00000508203.1:n.465G>T
ENST00000682567.1:n.513G>T
ENST00000683521.1:c.436G>T	ENSP00000506864.1:p.Gly146Ter
ENST00000684483.1:c.436G>T	ENSP00000507894.1:p.Gly146Ter
ENST00000366560.4:c.436G>T MANE Select	ENSP00000355518.4:p.Gly146Ter
ENST00000366560.3:c.436G>T	ENSP00000355518.3:p.Gly146Ter
ENST00000497042.1:n.132G>T
NM_000143.3:c.436G>T , LRG_504t1:c.436G>T	NP_000134.2:p.Gly146Ter
XM_011544132.1:c.208G>T	XP_011542434.1:p.Gly70Ter
XM_011544132.2:c.208G>T	XP_011542434.1:p.Gly70Ter
NM_000143.4:c.436G>T MANE Select	NP_000134.2:p.Gly146Ter