Canonical Allele Identifier: CA1969071982
Gene: F2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725913A= , CM000673.2:g.46725913A= GRCh38
NC_000011.9:g.46747463A= , CM000673.1:g.46747463A= GRCh37
NC_000011.8:g.46704039A= NCBI36
NG_008953.1:g.11721A= , LRG_551:g.11721A=

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.614A= MANE Select ENSP00000308541.5:p.Asn205=
ENST00000311907.9:c.614A= ENSP00000308541.5:p.Asn205=
ENST00000442468.1:c.584A= ENSP00000387413.1:p.Asn195=
ENST00000490274.1:n.394A=
ENST00000530231.5:c.614A= ENSP00000433907.1:p.Asn205=
NM_000506.3:c.614A= NP_000497.1:p.Asn205=
NM_000506.4:c.614A= , LRG_551t1:c.614A= NP_000497.1:p.Asn205=
NM_001311257.1:c.566A= NP_001298186.1:p.Asn189=
XR_428840.2:n.658A=
XR_428840.4:n.649A=
NM_000506.5:c.614A= MANE Select NP_000497.1:p.Asn205=
NM_001311257.2:c.566A= NP_001298186.1:p.Asn189=