Canonical Allele Identifier: CA5967083

Gene: F2

Linked Data

• dbSNP Id: rs772910933
• ExAC: 11:46747736 G / GATGA
• gnomAD v4: 11-46726186-G-GATGA
• MyVariant Identifiers: chr11:g.46747736_46747737insATGA (hg19) ; chr11:g.46726186_46726187insATGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726186_46726187insATGA , CM000673.2:g.46726186_46726187insATGA	GRCh38
NC_000011.9:g.46747736_46747737insATGA , CM000673.1:g.46747736_46747737insATGA	GRCh37
NC_000011.8:g.46704312_46704313insATGA	NCBI36
NG_008953.1:g.11994_11995insATGA , LRG_551:g.11994_11995insATGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+13_874+14insATGA MANE Select	ENSP00000308541.5:n.874+13_874+14insATGA
ENST00000311907.9:c.874+13_874+14insATGA	ENSP00000308541.5:n.874+13_874+14insATGA
ENST00000442468.1:c.844+13_844+14insATGA	ENSP00000387413.1:n.844+13_844+14insATGA
ENST00000530231.5:c.874+13_874+14insATGA	ENSP00000433907.1:n.874+13_874+14insATGA
NM_000506.3:c.874+13_874+14insATGA	NP_000497.1:n.874+13_874+14insATGA
NM_000506.4:c.874+13_874+14insATGA , LRG_551t1:c.874+13_874+14insATGA	NP_000497.1:n.874+13_874+14insATGA
NM_001311257.1:c.826+13_826+14insATGA	NP_001298186.1:n.826+13_826+14insATGA
XR_428840.2:n.918+13_918+14insATGA
XR_428840.4:n.909+13_909+14insATGA
NM_000506.5:c.874+13_874+14insATGA MANE Select	NP_000497.1:n.874+13_874+14insATGA
NM_001311257.2:c.826+13_826+14insATGA	NP_001298186.1:n.826+13_826+14insATGA