Canonical Allele Identifier: CA733642225

Gene: FH

Linked Data

• dbSNP Id: rs1207109633
• gnomAD v3: 1-241511929-A-G
• gnomAD v4: 1-241511929-A-G
• MyVariant Identifiers: chr1:g.241675229A>G (hg19) ; chr1:g.241511929A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241511929A>G , CM000663.2:g.241511929A>G	GRCh38
NC_000001.10:g.241675229A>G , CM000663.1:g.241675229A>G	GRCh37
NC_000001.9:g.239741852A>G	NCBI36
NG_012338.1:g.12826T>C , LRG_504:g.12826T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1058+38T>C
ENST00000682162.1:c.584+38T>C	ENSP00000508203.1:n.584+38T>C
ENST00000682567.1:n.632+38T>C
ENST00000683521.1:c.555+38T>C	ENSP00000506864.1:n.555+38T>C
ENST00000684483.1:c.555+38T>C	ENSP00000507894.1:n.555+38T>C
ENST00000366560.4:c.555+38T>C MANE Select	ENSP00000355518.4:n.555+38T>C
ENST00000366560.3:c.555+38T>C	ENSP00000355518.3:n.555+38T>C
ENST00000497042.1:n.289T>C
NM_000143.3:c.555+38T>C , LRG_504t1:c.555+38T>C	NP_000134.2:n.555+38T>C
XM_011544132.1:c.327+38T>C	XP_011542434.1:n.327+38T>C
XM_011544132.2:c.327+38T>C	XP_011542434.1:n.327+38T>C
NM_000143.4:c.555+38T>C MANE Select	NP_000134.2:n.555+38T>C