Canonical Allele Identifier: CA345442041

Gene: FH

Linked Data

• gnomAD v4: 1-241517308-T-G
• MyVariant Identifiers: chr1:g.241680608T>G (hg19) ; chr1:g.241517308T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241517308T>G , CM000663.2:g.241517308T>G	GRCh38
NC_000001.10:g.241680608T>G , CM000663.1:g.241680608T>G	GRCh37
NC_000001.9:g.239747231T>G	NCBI36
NG_012338.1:g.7447A>C , LRG_504:g.7447A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.644A>C
ENST00000682162.1:c.170A>C	ENSP00000508203.1:p.Lys57Thr
ENST00000682567.1:n.218A>C
ENST00000683521.1:c.141A>C	ENSP00000506864.1:p.Gln47His
ENST00000684483.1:c.141A>C	ENSP00000507894.1:p.Gln47His
ENST00000366560.4:c.141A>C MANE Select	ENSP00000355518.4:p.Gln47His
ENST00000366560.3:c.141A>C	ENSP00000355518.3:p.Gln47His
ENST00000493477.1:n.254A>C
NM_000143.3:c.141A>C , LRG_504t1:c.141A>C	NP_000134.2:p.Gln47His
XM_011544132.1:c.-88A>C	XP_011542434.1:n.-88A>C
XM_011544132.2:c.-88A>C	XP_011542434.1:n.-88A>C
NM_000143.4:c.141A>C MANE Select	NP_000134.2:p.Gln47His