Canonical Allele Identifier: CA560478642

Gene: F2R

Linked Data

• dbSNP Id: rs1466275892
• gnomAD v2: 5-76023396-A-G
• gnomAD v3: 5-76727571-A-G
• gnomAD v4: 5-76727571-A-G
• MyVariant Identifiers: chr5:g.76023396A>G (hg19) ; chr5:g.76727571A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76727571A>G , CM000667.2:g.76727571A>G	GRCh38
NC_000005.9:g.76023396A>G , CM000667.1:g.76023396A>G	GRCh37
NC_000005.8:g.76059152A>G	NCBI36
NG_032906.1:g.16529A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000319211.5:c.89-4743A>G MANE Select	ENSP00000321326.4:n.89-4743A>G
ENST00000319211.4:c.89-4743A>G	ENSP00000321326.4:n.89-4743A>G
NM_001311313.1:c.-397-1141A>G	NP_001298242.1:n.-397-1141A>G
NM_001992.3:c.89-4743A>G	NP_001983.2:n.89-4743A>G
NM_001992.4:c.89-4743A>G	NP_001983.2:n.89-4743A>G
NM_001992.5:c.89-4743A>G MANE Select	NP_001983.2:n.89-4743A>G
NM_001311313.2:c.-397-1141A>G	NP_001298242.1:n.-397-1141A>G