Canonical Allele Identifier: CA345441857

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241680550A>G (hg19) ; chr1:g.241517250A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241517250A>G , CM000663.2:g.241517250A>G	GRCh38
NC_000001.10:g.241680550A>G , CM000663.1:g.241680550A>G	GRCh37
NC_000001.9:g.239747173A>G	NCBI36
NG_012338.1:g.7505T>C , LRG_504:g.7505T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.702T>C
ENST00000682162.1:c.228T>C	ENSP00000508203.1:n.228T>C
ENST00000682567.1:n.276T>C
ENST00000683521.1:c.199T>C	ENSP00000506864.1:p.Tyr67His
ENST00000684483.1:c.199T>C	ENSP00000507894.1:p.Tyr67His
ENST00000366560.4:c.199T>C MANE Select	ENSP00000355518.4:p.Tyr67His
ENST00000366560.3:c.199T>C	ENSP00000355518.3:p.Tyr67His
ENST00000493477.1:n.312T>C
NM_000143.3:c.199T>C , LRG_504t1:c.199T>C	NP_000134.2:p.Tyr67His
XM_011544132.1:c.-30T>C	XP_011542434.1:n.-30T>C
XM_011544132.2:c.-30T>C	XP_011542434.1:n.-30T>C
NM_000143.4:c.199T>C MANE Select	NP_000134.2:p.Tyr67His