Canonical Allele Identifier: CA2697547764
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 2770926
ClinVar RCV Id: RCV003580904

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241504023_241504092del , CM000663.2:g.241504023_241504092del GRCh38
NC_000001.10:g.241667323_241667392del , CM000663.1:g.241667323_241667392del GRCh37
NC_000001.9:g.239733946_239734015del NCBI36
NG_012338.1:g.20663_20732del , LRG_504:g.20663_20732del

Transcript Alleles

HGVS Amino-acid Change
ENST00000493477.2:n.1561_1611+19del
ENST00000682162.1:c.1087_1137+19del
ENST00000682567.1:n.1135_1204del
ENST00000683521.1:c.1058_1108+19del
ENST00000684161.1:n.2273_2323+19del
ENST00000684483.1:c.*454_*504+19del
ENST00000366560.4:c.1058_1108+19del
ENST00000366560.3:c.1058_1108+19del
NM_000143.3:c.1058_1108+19del , LRG_504t1:c.1058_1108+19del
XM_011544132.1:c.830_880+19del
XM_011544132.2:c.830_880+19del
NM_000143.4:c.1058_1108+19del