Canonical Allele Identifier: CA424076009
Gene: FH HGNC NCBI

Linked Data

ClinVar Variation Id: 1758652
MyVariant Identifiers: chr1:g.241671903C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241508603C>T , CM000663.2:g.241508603C>T GRCh38
NC_000001.10:g.241671903C>T , CM000663.1:g.241671903C>T GRCh37
NC_000001.9:g.239738526C>T NCBI36
NG_012338.1:g.16152G>A , LRG_504:g.16152G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000493477.2:n.1241G>A
ENST00000682162.1:c.767G>A ENSP00000508203.1:n.767G>A
ENST00000682567.1:n.815G>A
ENST00000683521.1:c.738G>A ENSP00000506864.1:p.Gln246=
ENST00000684161.1:n.1953G>A
ENST00000684483.1:c.*134G>A ENSP00000507894.1:n.*134G>A
ENST00000366560.4:c.738G>A MANE Select ENSP00000355518.4:p.Gln246=
ENST00000366560.3:c.738G>A ENSP00000355518.3:p.Gln246=
NM_000143.3:c.738G>A , LRG_504t1:c.738G>A NP_000134.2:p.Gln246=
XM_011544132.1:c.510G>A XP_011542434.1:p.Gln170=
XM_011544132.2:c.510G>A XP_011542434.1:p.Gln170=
NM_000143.4:c.738G>A MANE Select NP_000134.2:p.Gln246=