Canonical Allele Identifier: CA121029839

Gene: F2R

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76727669A>G , CM000667.2:g.76727669A>G	GRCh38
NC_000005.9:g.76023494A>G , CM000667.1:g.76023494A>G	GRCh37
NC_000005.8:g.76059250A>G	NCBI36
NG_032906.1:g.16627A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319211.5:c.89-4645A>G MANE Select	ENSP00000321326.4:n.89-4645A>G
ENST00000319211.4:c.89-4645A>G	ENSP00000321326.4:n.89-4645A>G
NM_001311313.1:c.-397-1043A>G	NP_001298242.1:n.-397-1043A>G
NM_001992.3:c.89-4645A>G	NP_001983.2:n.89-4645A>G
NM_001992.4:c.89-4645A>G	NP_001983.2:n.89-4645A>G
NM_001992.5:c.89-4645A>G MANE Select	NP_001983.2:n.89-4645A>G
NM_001311313.2:c.-397-1043A>G	NP_001298242.1:n.-397-1043A>G