Canonical Allele Identifier: CA937604685

Gene: F2

Linked Data

• dbSNP Id: rs2064885652
• gnomAD v3: 11-46727928-C-CA
• gnomAD v4: 11-46727928-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46727928_46727929insA , CM000673.2:g.46727928_46727929insA	GRCh38
NC_000011.9:g.46749478_46749479insA , CM000673.1:g.46749478_46749479insA	GRCh37
NC_000011.8:g.46706054_46706055insA	NCBI36
NG_008953.1:g.13736_13737insA , LRG_551:g.13736_13737insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1131-68_1131-67insA MANE Select	ENSP00000308541.5:n.1131-68_1131-67insA
ENST00000311907.9:c.1131-68_1131-67insA	ENSP00000308541.5:n.1131-68_1131-67insA
ENST00000530231.5:c.1131-68_1131-67insA	ENSP00000433907.1:n.1131-68_1131-67insA
NM_000506.3:c.1131-68_1131-67insA	NP_000497.1:n.1131-68_1131-67insA
NM_000506.4:c.1131-68_1131-67insA , LRG_551t1:c.1131-68_1131-67insA	NP_000497.1:n.1131-68_1131-67insA
NM_001311257.1:c.1083-68_1083-67insA	NP_001298186.1:n.1083-68_1083-67insA
XR_428840.2:n.1175-68_1175-67insA
XR_428840.4:n.1166-68_1166-67insA
NM_000506.5:c.1131-68_1131-67insA MANE Select	NP_000497.1:n.1131-68_1131-67insA
NM_001311257.2:c.1083-68_1083-67insA	NP_001298186.1:n.1083-68_1083-67insA