Canonical Allele Identifier: CA1969072428
Gene: F2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46726231A= , CM000673.2:g.46726231A= GRCh38
NC_000011.9:g.46747781A= , CM000673.1:g.46747781A= GRCh37
NC_000011.8:g.46704357A= NCBI36
NG_008953.1:g.12039A= , LRG_551:g.12039A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.874+58A= MANE Select ENSP00000308541.5:n.874+58A=
ENST00000311907.9:c.874+58A= ENSP00000308541.5:n.874+58A=
ENST00000442468.1:c.844+58A= ENSP00000387413.1:n.844+58A=
ENST00000530231.5:c.874+58A= ENSP00000433907.1:n.874+58A=
NM_000506.3:c.874+58A= NP_000497.1:n.874+58A=
NM_000506.4:c.874+58A= , LRG_551t1:c.874+58A= NP_000497.1:n.874+58A=
NM_001311257.1:c.826+58A= NP_001298186.1:n.826+58A=
XR_428840.2:n.918+58A=
XR_428840.4:n.909+58A=
NM_000506.5:c.874+58A= MANE Select NP_000497.1:n.874+58A=
NM_001311257.2:c.826+58A= NP_001298186.1:n.826+58A=
Search 100 bp 5'
Search 100 bp 3'