Canonical Allele Identifier: CA733680033

Gene: FH

Linked Data

• dbSNP Id: rs1487330690
• gnomAD v3: 1-241502703-G-T
• gnomAD v4: 1-241502703-G-T
• MyVariant Identifiers: chr1:g.241666003G>T (hg19) ; chr1:g.241502703G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502703G>T , CM000663.2:g.241502703G>T	GRCh38
NC_000001.10:g.241666003G>T , CM000663.1:g.241666003G>T	GRCh37
NC_000001.9:g.239732626G>T	NCBI36
NG_012338.1:g.22052C>A , LRG_504:g.22052C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1612-133C>A
ENST00000682162.1:c.1138-133C>A	ENSP00000508203.1:n.1138-133C>A
ENST00000682567.1:n.2524C>A
ENST00000683521.1:c.1109-133C>A	ENSP00000506864.1:n.1109-133C>A
ENST00000684161.1:n.2324-133C>A
ENST00000684483.1:c.*505-133C>A	ENSP00000507894.1:n.*505-133C>A
ENST00000366560.4:c.1109-133C>A MANE Select	ENSP00000355518.4:n.1109-133C>A
ENST00000366560.3:c.1109-133C>A	ENSP00000355518.3:n.1109-133C>A
NM_000143.3:c.1109-133C>A , LRG_504t1:c.1109-133C>A	NP_000134.2:n.1109-133C>A
XM_011544132.1:c.881-133C>A	XP_011542434.1:n.881-133C>A
XM_011544132.2:c.881-133C>A	XP_011542434.1:n.881-133C>A
NM_000143.4:c.1109-133C>A MANE Select	NP_000134.2:n.1109-133C>A