Canonical Allele Identifier: CA814107776

Gene: F2R

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76728994A>T , CM000667.2:g.76728994A>T	GRCh38
NC_000005.9:g.76024819A>T , CM000667.1:g.76024819A>T	GRCh37
NC_000005.8:g.76060575A>T	NCBI36
NG_032906.1:g.17952A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000319211.5:c.89-3320A>T MANE Select	ENSP00000321326.4:n.89-3320A>T
ENST00000319211.4:c.89-3320A>T	ENSP00000321326.4:n.89-3320A>T
NM_001311313.1:c.-276+161A>T	NP_001298242.1:n.-276+161A>T
NM_001992.3:c.89-3320A>T	NP_001983.2:n.89-3320A>T
NM_001992.4:c.89-3320A>T	NP_001983.2:n.89-3320A>T
NM_001992.5:c.89-3320A>T MANE Select	NP_001983.2:n.89-3320A>T
NM_001311313.2:c.-276+161A>T	NP_001298242.1:n.-276+161A>T