Canonical Allele Identifier: CA2613334361
Gene: F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725728A>G , CM000673.2:g.46725728A>G GRCh38
NC_000011.9:g.46747278A>G , CM000673.1:g.46747278A>G GRCh37
NC_000011.8:g.46703854A>G NCBI36
NG_008953.1:g.11536A>G , LRG_551:g.11536A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.560-131A>G MANE Select ENSP00000308541.5:n.560-131A>G
ENST00000311907.9:c.560-131A>G ENSP00000308541.5:n.560-131A>G
ENST00000442468.1:c.530-131A>G ENSP00000387413.1:n.530-131A>G
ENST00000490274.1:n.340-131A>G
ENST00000530231.5:c.560-131A>G ENSP00000433907.1:n.560-131A>G
NM_000506.3:c.560-131A>G NP_000497.1:n.560-131A>G
NM_000506.4:c.560-131A>G , LRG_551t1:c.560-131A>G NP_000497.1:n.560-131A>G
NM_001311257.1:c.512-131A>G NP_001298186.1:n.512-131A>G
XR_428840.2:n.604-131A>G
XR_428840.4:n.595-131A>G
NM_000506.5:c.560-131A>G MANE Select NP_000497.1:n.560-131A>G
NM_001311257.2:c.512-131A>G NP_001298186.1:n.512-131A>G