Canonical Allele Identifier: CA345440046

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241675359C>A (hg19) ; chr1:g.241512059C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512059C>A , CM000663.2:g.241512059C>A	GRCh38
NC_000001.10:g.241675359C>A , CM000663.1:g.241675359C>A	GRCh37
NC_000001.9:g.239741982C>A	NCBI36
NG_012338.1:g.12696G>T , LRG_504:g.12696G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.966G>T
ENST00000682162.1:c.492G>T	ENSP00000508203.1:n.492G>T
ENST00000682567.1:n.540G>T
ENST00000683521.1:c.463G>T	ENSP00000506864.1:p.Glu155Ter
ENST00000684483.1:c.463G>T	ENSP00000507894.1:p.Glu155Ter
ENST00000366560.4:c.463G>T MANE Select	ENSP00000355518.4:p.Glu155Ter
ENST00000366560.3:c.463G>T	ENSP00000355518.3:p.Glu155Ter
ENST00000497042.1:n.159G>T
NM_000143.3:c.463G>T , LRG_504t1:c.463G>T	NP_000134.2:p.Glu155Ter
XM_011544132.1:c.235G>T	XP_011542434.1:p.Glu79Ter
XM_011544132.2:c.235G>T	XP_011542434.1:p.Glu79Ter
NM_000143.4:c.463G>T MANE Select	NP_000134.2:p.Glu155Ter