Canonical Allele Identifier: CA5967195

Gene: F2

Linked Data

• dbSNP Id: rs771893995
• ExAC: 11:46749520 C / CGCA
• gnomAD v2: 11-46749520-C-CGCA
• gnomAD v4: 11-46727970-C-CGCA
• MyVariant Identifiers: chr11:g.46749520_46749521insGCA (hg19) ; chr11:g.46727970_46727971insGCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46727970_46727971insGCA , CM000673.2:g.46727970_46727971insGCA	GRCh38
NC_000011.9:g.46749520_46749521insGCA , CM000673.1:g.46749520_46749521insGCA	GRCh37
NC_000011.8:g.46706096_46706097insGCA	NCBI36
NG_008953.1:g.13778_13779insGCA , LRG_551:g.13778_13779insGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1131-26_1131-25insGCA MANE Select	ENSP00000308541.5:n.1131-26_1131-25insGCA
ENST00000311907.9:c.1131-26_1131-25insGCA	ENSP00000308541.5:n.1131-26_1131-25insGCA
ENST00000530231.5:c.1131-26_1131-25insGCA	ENSP00000433907.1:n.1131-26_1131-25insGCA
NM_000506.3:c.1131-26_1131-25insGCA	NP_000497.1:n.1131-26_1131-25insGCA
NM_000506.4:c.1131-26_1131-25insGCA , LRG_551t1:c.1131-26_1131-25insGCA	NP_000497.1:n.1131-26_1131-25insGCA
NM_001311257.1:c.1083-26_1083-25insGCA	NP_001298186.1:n.1083-26_1083-25insGCA
XR_428840.2:n.1175-26_1175-25insGCA
XR_428840.4:n.1166-26_1166-25insGCA
NM_000506.5:c.1131-26_1131-25insGCA MANE Select	NP_000497.1:n.1131-26_1131-25insGCA
NM_001311257.2:c.1083-26_1083-25insGCA	NP_001298186.1:n.1083-26_1083-25insGCA