Canonical Allele Identifier: CA424076602

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241680563C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241517263C>G , CM000663.2:g.241517263C>G	GRCh38
NC_000001.10:g.241680563C>G , CM000663.1:g.241680563C>G	GRCh37
NC_000001.9:g.239747186C>G	NCBI36
NG_012338.1:g.7492G>C , LRG_504:g.7492G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.689G>C
ENST00000682162.1:c.215G>C	ENSP00000508203.1:n.215G>C
ENST00000682567.1:n.263G>C
ENST00000683521.1:c.186G>C	ENSP00000506864.1:p.Val62=
ENST00000684483.1:c.186G>C	ENSP00000507894.1:p.Val62=
ENST00000366560.4:c.186G>C MANE Select	ENSP00000355518.4:p.Val62=
ENST00000366560.3:c.186G>C	ENSP00000355518.3:p.Val62=
ENST00000493477.1:n.299G>C
NM_000143.3:c.186G>C , LRG_504t1:c.186G>C	NP_000134.2:p.Val62=
XM_011544132.1:c.-43G>C	XP_011542434.1:n.-43G>C
XM_011544132.2:c.-43G>C	XP_011542434.1:n.-43G>C
NM_000143.4:c.186G>C MANE Select	NP_000134.2:p.Val62=