Canonical Allele Identifier: CA473871026
Gene: F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.46745007A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46723457A>C , CM000673.2:g.46723457A>C GRCh38
NC_000011.9:g.46745007A>C , CM000673.1:g.46745007A>C GRCh37
NC_000011.8:g.46701583A>C NCBI36
NG_008953.1:g.9265A>C , LRG_551:g.9265A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.498A>C MANE Select ENSP00000308541.5:p.Gly166=
ENST00000311907.9:c.498A>C ENSP00000308541.5:p.Gly166=
ENST00000442468.1:c.468A>C ENSP00000387413.1:p.Gly156=
ENST00000490274.1:n.278A>C
ENST00000530231.5:c.498A>C ENSP00000433907.1:p.Gly166=
NM_000506.3:c.498A>C NP_000497.1:p.Gly166=
NM_000506.4:c.498A>C , LRG_551t1:c.498A>C NP_000497.1:p.Gly166=
NM_001311257.1:c.450A>C NP_001298186.1:p.Gly150=
XR_428840.2:n.542A>C
XR_428840.4:n.533A>C
NM_000506.5:c.498A>C MANE Select NP_000497.1:p.Gly166=
NM_001311257.2:c.450A>C NP_001298186.1:p.Gly150=