Canonical Allele Identifier: CA1969071962
Gene: F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725902C= , CM000673.2:g.46725902C= GRCh38
NC_000011.9:g.46747452C= , CM000673.1:g.46747452C= GRCh37
NC_000011.8:g.46704028C= NCBI36
NG_008953.1:g.11710C= , LRG_551:g.11710C=

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.603C= MANE Select ENSP00000308541.5:p.Gly201=
ENST00000311907.9:c.603C= ENSP00000308541.5:p.Gly201=
ENST00000442468.1:c.573C= ENSP00000387413.1:p.Gly191=
ENST00000490274.1:n.383C=
ENST00000530231.5:c.603C= ENSP00000433907.1:p.Gly201=
NM_000506.3:c.603C= NP_000497.1:p.Gly201=
NM_000506.4:c.603C= , LRG_551t1:c.603C= NP_000497.1:p.Gly201=
NM_001311257.1:c.555C= NP_001298186.1:p.Gly185=
XR_428840.2:n.647C=
XR_428840.4:n.638C=
NM_000506.5:c.603C= MANE Select NP_000497.1:p.Gly201=
NM_001311257.2:c.555C= NP_001298186.1:p.Gly185=