Canonical Allele Identifier: CA1969071825
Gene: F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725810C>T , CM000673.2:g.46725810C>T GRCh38
NC_000011.9:g.46747360C>T , CM000673.1:g.46747360C>T GRCh37
NC_000011.8:g.46703936C>T NCBI36
NG_008953.1:g.11618C>T , LRG_551:g.11618C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.560-49C>T MANE Select ENSP00000308541.5:p.=
ENST00000311907.9:c.560-49C>T ENSP00000308541.5:p.=
ENST00000442468.1:c.530-49C>T ENSP00000387413.1:p.=
ENST00000490274.1:n.340-49C>T
ENST00000530231.5:c.560-49C>T ENSP00000433907.1:p.=
NM_000506.3:c.560-49C>T NP_000497.1:p.=
NM_000506.4:c.560-49C>T , LRG_551t1:c.560-49C>T NP_000497.1:p.=
NM_001311257.1:c.512-49C>T NP_001298186.1:p.=
XR_428840.2:n.604-49C>T
XR_428840.4:n.595-49C>T
NM_000506.5:c.560-49C>T MANE Select NP_000497.1:p.=
NM_001311257.2:c.512-49C>T NP_001298186.1:p.=