Canonical Allele Identifier: CA937603957

Gene: F2

Linked Data

• dbSNP Id: rs2064867358
• gnomAD v3: 11-46725733-CAG-C
• gnomAD v4: 11-46725733-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725738_46725739del , CM000673.2:g.46725738_46725739del	GRCh38
NC_000011.9:g.46747288_46747289del , CM000673.1:g.46747288_46747289del	GRCh37
NC_000011.8:g.46703864_46703865del	NCBI36
NG_008953.1:g.11546_11547del , LRG_551:g.11546_11547del

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.560-121_560-120del MANE Select	ENSP00000308541.5:n.560-121_560-120del
ENST00000311907.9:c.560-121_560-120del	ENSP00000308541.5:n.560-121_560-120del
ENST00000442468.1:c.530-121_530-120del	ENSP00000387413.1:n.530-121_530-120del
ENST00000490274.1:n.340-121_340-120del
ENST00000530231.5:c.560-121_560-120del	ENSP00000433907.1:n.560-121_560-120del
NM_000506.3:c.560-121_560-120del	NP_000497.1:n.560-121_560-120del
NM_000506.4:c.560-121_560-120del , LRG_551t1:c.560-121_560-120del	NP_000497.1:n.560-121_560-120del
NM_001311257.1:c.512-121_512-120del	NP_001298186.1:n.512-121_512-120del
XR_428840.2:n.604-121_604-120del
XR_428840.4:n.595-121_595-120del
NM_000506.5:c.560-121_560-120del MANE Select	NP_000497.1:n.560-121_560-120del
NM_001311257.2:c.512-121_512-120del	NP_001298186.1:n.512-121_512-120del