Canonical Allele Identifier: CA937604166

Gene: F2

Linked Data

• dbSNP Id: rs2064873123
• gnomAD v3: 11-46726395-C-G
• gnomAD v4: 11-46726395-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726395C>G , CM000673.2:g.46726395C>G	GRCh38
NC_000011.9:g.46747945C>G , CM000673.1:g.46747945C>G	GRCh37
NC_000011.8:g.46704521C>G	NCBI36
NG_008953.1:g.12203C>G , LRG_551:g.12203C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.875-103C>G MANE Select	ENSP00000308541.5:n.875-103C>G
ENST00000311907.9:c.875-103C>G	ENSP00000308541.5:n.875-103C>G
ENST00000442468.1:c.845-103C>G	ENSP00000387413.1:n.845-103C>G
ENST00000530231.5:c.875-103C>G	ENSP00000433907.1:n.875-103C>G
NM_000506.3:c.875-103C>G	NP_000497.1:n.875-103C>G
NM_000506.4:c.875-103C>G , LRG_551t1:c.875-103C>G	NP_000497.1:n.875-103C>G
NM_001311257.1:c.827-103C>G	NP_001298186.1:n.827-103C>G
XR_428840.2:n.919-103C>G
XR_428840.4:n.910-103C>G
NM_000506.5:c.875-103C>G MANE Select	NP_000497.1:n.875-103C>G
NM_001311257.2:c.827-103C>G	NP_001298186.1:n.827-103C>G