Canonical Allele Identifier: CA345436369

Gene: FH

Linked Data

• gnomAD v4: 1-241500461-C-T
• MyVariant Identifiers: chr1:g.241663761C>T (hg19) ; chr1:g.241500461C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241500461C>T , CM000663.2:g.241500461C>T	GRCh38
NC_000001.10:g.241663761C>T , CM000663.1:g.241663761C>T	GRCh37
NC_000001.9:g.239730384C>T	NCBI36
NG_012338.1:g.24294G>A , LRG_504:g.24294G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1869G>A
ENST00000682162.1:c.1395G>A	ENSP00000508203.1:n.1395G>A
ENST00000682567.1:n.4766G>A
ENST00000683521.1:c.1366G>A	ENSP00000506864.1:p.Val456Met
ENST00000684161.1:n.2581G>A
ENST00000684483.1:c.*762G>A	ENSP00000507894.1:n.*762G>A
ENST00000366560.4:c.1366G>A MANE Select	ENSP00000355518.4:p.Val456Met
ENST00000366560.3:c.1366G>A	ENSP00000355518.3:p.Val456Met
NM_000143.3:c.1366G>A , LRG_504t1:c.1366G>A	NP_000134.2:p.Val456Met
XM_011544132.1:c.1138G>A	XP_011542434.1:p.Val380Met
XM_011544132.2:c.1138G>A	XP_011542434.1:p.Val380Met
NM_000143.4:c.1366G>A MANE Select	NP_000134.2:p.Val456Met