Canonical Allele Identifier: CA474043848
Gene: F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.46748328A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46726778A>G , CM000673.2:g.46726778A>G GRCh38
NC_000011.9:g.46748328A>G , CM000673.1:g.46748328A>G GRCh37
NC_000011.8:g.46704904A>G NCBI36
NG_008953.1:g.12586A>G , LRG_551:g.12586A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.1071A>G MANE Select ENSP00000308541.5:p.Glu357=
ENST00000311907.9:c.1071A>G ENSP00000308541.5:p.Glu357=
ENST00000530231.5:c.1071A>G ENSP00000433907.1:p.Glu357=
NM_000506.3:c.1071A>G NP_000497.1:p.Glu357=
NM_000506.4:c.1071A>G , LRG_551t1:c.1071A>G NP_000497.1:p.Glu357=
NM_001311257.1:c.1023A>G NP_001298186.1:p.Glu341=
XR_428840.2:n.1115A>G
XR_428840.4:n.1106A>G
NM_000506.5:c.1071A>G MANE Select NP_000497.1:p.Glu357=
NM_001311257.2:c.1023A>G NP_001298186.1:p.Glu341=