Canonical Allele Identifier: CA40327902

Gene: FH

Linked Data

• dbSNP Id: rs1040420520
• gnomAD v3: 1-241503985-A-G
• gnomAD v4: 1-241503985-A-G
• MyVariant Identifiers: chr1:g.241667285A>G (hg19) ; chr1:g.241503985A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241503985A>G , CM000663.2:g.241503985A>G	GRCh38
NC_000001.10:g.241667285A>G , CM000663.1:g.241667285A>G	GRCh37
NC_000001.9:g.239733908A>G	NCBI36
NG_012338.1:g.20770T>C , LRG_504:g.20770T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1611+57T>C
ENST00000682162.1:c.1137+57T>C	ENSP00000508203.1:n.1137+57T>C
ENST00000682567.1:n.1242T>C
ENST00000683521.1:c.1108+57T>C	ENSP00000506864.1:n.1108+57T>C
ENST00000684161.1:n.2323+57T>C
ENST00000684483.1:c.*504+57T>C	ENSP00000507894.1:n.*504+57T>C
ENST00000366560.4:c.1108+57T>C MANE Select	ENSP00000355518.4:n.1108+57T>C
ENST00000366560.3:c.1108+57T>C	ENSP00000355518.3:n.1108+57T>C
NM_000143.3:c.1108+57T>C , LRG_504t1:c.1108+57T>C	NP_000134.2:n.1108+57T>C
XM_011544132.1:c.880+57T>C	XP_011542434.1:n.880+57T>C
XM_011544132.2:c.880+57T>C	XP_011542434.1:n.880+57T>C
NM_000143.4:c.1108+57T>C MANE Select	NP_000134.2:n.1108+57T>C