Canonical Allele Identifier: CA5966966
Gene: F2 HGNC NCBI

Linked Data

dbSNP Id: rs369468882

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46723460C>G , CM000673.2:g.46723460C>G GRCh38
NC_000011.9:g.46745010C>G , CM000673.1:g.46745010C>G GRCh37
NC_000011.8:g.46701586C>G NCBI36
NG_008953.1:g.9268C>G , LRG_551:g.9268C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.501C>G MANE Select ENSP00000308541.5:p.Pro167=
ENST00000311907.9:c.501C>G ENSP00000308541.5:p.Pro167=
ENST00000442468.1:c.471C>G ENSP00000387413.1:p.Pro157=
ENST00000490274.1:n.281C>G
ENST00000530231.5:c.501C>G ENSP00000433907.1:p.Pro167=
NM_000506.3:c.501C>G NP_000497.1:p.Pro167=
NM_000506.4:c.501C>G , LRG_551t1:c.501C>G NP_000497.1:p.Pro167=
NM_001311257.1:c.453C>G NP_001298186.1:p.Pro151=
XR_428840.2:n.545C>G
XR_428840.4:n.536C>G
NM_000506.5:c.501C>G MANE Select NP_000497.1:p.Pro167=
NM_001311257.2:c.453C>G NP_001298186.1:p.Pro151=