Canonical Allele Identifier: CA1077703165

Gene: F2R

Linked Data

• dbSNP Id: rs1748587981
• gnomAD v3: 5-76727605-C-T
• gnomAD v4: 5-76727605-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76727605C>T , CM000667.2:g.76727605C>T	GRCh38
NC_000005.9:g.76023430C>T , CM000667.1:g.76023430C>T	GRCh37
NC_000005.8:g.76059186C>T	NCBI36
NG_032906.1:g.16563C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000319211.5:c.89-4709C>T MANE Select	ENSP00000321326.4:n.89-4709C>T
ENST00000319211.4:c.89-4709C>T	ENSP00000321326.4:n.89-4709C>T
NM_001311313.1:c.-397-1107C>T	NP_001298242.1:n.-397-1107C>T
NM_001992.3:c.89-4709C>T	NP_001983.2:n.89-4709C>T
NM_001992.4:c.89-4709C>T	NP_001983.2:n.89-4709C>T
NM_001992.5:c.89-4709C>T MANE Select	NP_001983.2:n.89-4709C>T
NM_001311313.2:c.-397-1107C>T	NP_001298242.1:n.-397-1107C>T