Canonical Allele Identifier: CA733642772

Gene: FH

Linked Data

• dbSNP Id: rs1213595945
• MyVariant Identifiers: chr1:g.241675626A>G (hg19) ; chr1:g.241512326A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512326A>G , CM000663.2:g.241512326A>G	GRCh38
NC_000001.10:g.241675626A>G , CM000663.1:g.241675626A>G	GRCh37
NC_000001.9:g.239742249A>G	NCBI36
NG_012338.1:g.12429T>C , LRG_504:g.12429T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.882-183T>C
ENST00000682162.1:c.408-183T>C	ENSP00000508203.1:n.408-183T>C
ENST00000682567.1:n.456-183T>C
ENST00000683521.1:c.379-183T>C	ENSP00000506864.1:n.379-183T>C
ENST00000684483.1:c.379-183T>C	ENSP00000507894.1:n.379-183T>C
ENST00000366560.4:c.379-183T>C MANE Select	ENSP00000355518.4:n.379-183T>C
ENST00000366560.3:c.379-183T>C	ENSP00000355518.3:n.379-183T>C
ENST00000497042.1:n.75-183T>C
NM_000143.3:c.379-183T>C , LRG_504t1:c.379-183T>C	NP_000134.2:n.379-183T>C
XM_011544132.1:c.151-183T>C	XP_011542434.1:n.151-183T>C
XM_011544132.2:c.151-183T>C	XP_011542434.1:n.151-183T>C
NM_000143.4:c.379-183T>C MANE Select	NP_000134.2:n.379-183T>C