Canonical Allele Identifier: CA345440067

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241675367T>G (hg19) ; chr1:g.241512067T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512067T>G , CM000663.2:g.241512067T>G	GRCh38
NC_000001.10:g.241675367T>G , CM000663.1:g.241675367T>G	GRCh37
NC_000001.9:g.239741990T>G	NCBI36
NG_012338.1:g.12688A>C , LRG_504:g.12688A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.958A>C
ENST00000682162.1:c.484A>C	ENSP00000508203.1:n.484A>C
ENST00000682567.1:n.532A>C
ENST00000683521.1:c.455A>C	ENSP00000506864.1:p.Asn152Thr
ENST00000684483.1:c.455A>C	ENSP00000507894.1:p.Asn152Thr
ENST00000366560.4:c.455A>C MANE Select	ENSP00000355518.4:p.Asn152Thr
ENST00000366560.3:c.455A>C	ENSP00000355518.3:p.Asn152Thr
ENST00000497042.1:n.151A>C
NM_000143.3:c.455A>C , LRG_504t1:c.455A>C	NP_000134.2:p.Asn152Thr
XM_011544132.1:c.227A>C	XP_011542434.1:p.Asn76Thr
XM_011544132.2:c.227A>C	XP_011542434.1:p.Asn76Thr
NM_000143.4:c.455A>C MANE Select	NP_000134.2:p.Asn152Thr