Canonical Allele Identifier: CA221651752
Gene: F2 HGNC NCBI

Linked Data

dbSNP Id: rs931170073

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725820C>G , CM000673.2:g.46725820C>G GRCh38
NC_000011.9:g.46747370C>G , CM000673.1:g.46747370C>G GRCh37
NC_000011.8:g.46703946C>G NCBI36
NG_008953.1:g.11628C>G , LRG_551:g.11628C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.560-39C>G MANE Select ENSP00000308541.5:n.560-39C>G
ENST00000311907.9:c.560-39C>G ENSP00000308541.5:n.560-39C>G
ENST00000442468.1:c.530-39C>G ENSP00000387413.1:n.530-39C>G
ENST00000490274.1:n.340-39C>G
ENST00000530231.5:c.560-39C>G ENSP00000433907.1:n.560-39C>G
NM_000506.3:c.560-39C>G NP_000497.1:n.560-39C>G
NM_000506.4:c.560-39C>G , LRG_551t1:c.560-39C>G NP_000497.1:n.560-39C>G
NM_001311257.1:c.512-39C>G NP_001298186.1:n.512-39C>G
XR_428840.2:n.604-39C>G
XR_428840.4:n.595-39C>G
NM_000506.5:c.560-39C>G MANE Select NP_000497.1:n.560-39C>G
NM_001311257.2:c.512-39C>G NP_001298186.1:n.512-39C>G