Canonical Allele Identifier: CA5967003
Gene: F2 HGNC NCBI

Linked Data

dbSNP Id: rs772477768

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725814T>C , CM000673.2:g.46725814T>C GRCh38
NC_000011.9:g.46747364T>C , CM000673.1:g.46747364T>C GRCh37
NC_000011.8:g.46703940T>C NCBI36
NG_008953.1:g.11622T>C , LRG_551:g.11622T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.560-45T>C MANE Select ENSP00000308541.5:n.560-45T>C
ENST00000311907.9:c.560-45T>C ENSP00000308541.5:n.560-45T>C
ENST00000442468.1:c.530-45T>C ENSP00000387413.1:n.530-45T>C
ENST00000490274.1:n.340-45T>C
ENST00000530231.5:c.560-45T>C ENSP00000433907.1:n.560-45T>C
NM_000506.3:c.560-45T>C NP_000497.1:n.560-45T>C
NM_000506.4:c.560-45T>C , LRG_551t1:c.560-45T>C NP_000497.1:n.560-45T>C
NM_001311257.1:c.512-45T>C NP_001298186.1:n.512-45T>C
XR_428840.2:n.604-45T>C
XR_428840.4:n.595-45T>C
NM_000506.5:c.560-45T>C MANE Select NP_000497.1:n.560-45T>C
NM_001311257.2:c.512-45T>C NP_001298186.1:n.512-45T>C