Canonical Allele Identifier: CA1229580586
Gene: FH HGNC NCBI

Linked Data

dbSNP Id: rs1659986450

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.241508532G>C , CM000663.2:g.241508532G>C GRCh38
NC_000001.10:g.241671832G>C , CM000663.1:g.241671832G>C GRCh37
NC_000001.9:g.239738455G>C NCBI36
NG_012338.1:g.16223C>G , LRG_504:g.16223C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000493477.2:n.1241+71C>G
ENST00000682162.1:c.767+71C>G ENSP00000508203.1:n.767+71C>G
ENST00000682567.1:n.815+71C>G
ENST00000683521.1:c.738+71C>G ENSP00000506864.1:n.738+71C>G
ENST00000684161.1:n.1953+71C>G
ENST00000684483.1:c.*134+71C>G ENSP00000507894.1:n.*134+71C>G
ENST00000366560.4:c.738+71C>G MANE Select ENSP00000355518.4:n.738+71C>G
ENST00000366560.3:c.738+71C>G ENSP00000355518.3:n.738+71C>G
NM_000143.3:c.738+71C>G , LRG_504t1:c.738+71C>G NP_000134.2:n.738+71C>G
XM_011544132.1:c.510+71C>G XP_011542434.1:n.510+71C>G
XM_011544132.2:c.510+71C>G XP_011542434.1:n.510+71C>G
NM_000143.4:c.738+71C>G MANE Select NP_000134.2:n.738+71C>G