Canonical Allele Identifier: CA11972658

Gene: F2R

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76718175C>A , CM000667.2:g.76718175C>A	GRCh38
NC_000005.9:g.76014000C>A , CM000667.1:g.76014000C>A	GRCh37
NC_000005.8:g.76049756C>A	NCBI36
NG_032906.1:g.7133C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319211.5:c.88+1780C>A MANE Select	ENSP00000321326.4:n.88+1780C>A
ENST00000319211.4:c.88+1780C>A	ENSP00000321326.4:n.88+1780C>A
NM_001311313.1:c.-398+1780C>A	NP_001298242.1:n.-398+1780C>A
NM_001992.3:c.88+1780C>A	NP_001983.2:n.88+1780C>A
NM_001992.4:c.88+1780C>A	NP_001983.2:n.88+1780C>A
NM_001992.5:c.88+1780C>A MANE Select	NP_001983.2:n.88+1780C>A
NM_001311313.2:c.-398+1780C>A	NP_001298242.1:n.-398+1780C>A