Canonical Allele Identifier: CA424076014
Gene: FH HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.241671909A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241508609A>T , CM000663.2:g.241508609A>T GRCh38
NC_000001.10:g.241671909A>T , CM000663.1:g.241671909A>T GRCh37
NC_000001.9:g.239738532A>T NCBI36
NG_012338.1:g.16146T>A , LRG_504:g.16146T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000493477.2:n.1235T>A
ENST00000682162.1:c.761T>A ENSP00000508203.1:n.761T>A
ENST00000682567.1:n.809T>A
ENST00000683521.1:c.732T>A ENSP00000506864.1:p.Leu244=
ENST00000684161.1:n.1947T>A
ENST00000684483.1:c.*128T>A ENSP00000507894.1:n.*128T>A
ENST00000366560.4:c.732T>A MANE Select ENSP00000355518.4:p.Leu244=
ENST00000366560.3:c.732T>A ENSP00000355518.3:p.Leu244=
NM_000143.3:c.732T>A , LRG_504t1:c.732T>A NP_000134.2:p.Leu244=
XM_011544132.1:c.504T>A XP_011542434.1:p.Leu168=
XM_011544132.2:c.504T>A XP_011542434.1:p.Leu168=
NM_000143.4:c.732T>A MANE Select NP_000134.2:p.Leu244=