Canonical Allele Identifier: CA2525295785
Gene: F2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76727571_76727572insAT , CM000667.2:g.76727571_76727572insAT GRCh38
NC_000005.9:g.76023396_76023397insAT , CM000667.1:g.76023396_76023397insAT GRCh37
NC_000005.8:g.76059152_76059153insAT NCBI36
NG_032906.1:g.16529_16530insAT

Transcript Alleles

HGVS Amino-acid change
ENST00000319211.5:c.89-4743_89-4742insAT MANE Select ENSP00000321326.4:n.89-4743_89-4742insAT
ENST00000319211.4:c.89-4743_89-4742insAT ENSP00000321326.4:n.89-4743_89-4742insAT
NM_001311313.1:c.-397-1141_-397-1140insAT NP_001298242.1:n.-397-1141_-397-1140insAT...
NM_001992.3:c.89-4743_89-4742insAT NP_001983.2:n.89-4743_89-4742insAT
NM_001992.4:c.89-4743_89-4742insAT NP_001983.2:n.89-4743_89-4742insAT
NM_001992.5:c.89-4743_89-4742insAT MANE Select NP_001983.2:n.89-4743_89-4742insAT
NM_001311313.2:c.-397-1141_-397-1140insAT NP_001298242.1:n.-397-1141_-397-1140insAT...