Canonical Allele Identifier: CA2613335059

Gene: F2

Linked Data

• gnomAD v4: 11-46726368-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726368G>A , CM000673.2:g.46726368G>A	GRCh38
NC_000011.9:g.46747918G>A , CM000673.1:g.46747918G>A	GRCh37
NC_000011.8:g.46704494G>A	NCBI36
NG_008953.1:g.12176G>A , LRG_551:g.12176G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.875-130G>A MANE Select	ENSP00000308541.5:n.875-130G>A
ENST00000311907.9:c.875-130G>A	ENSP00000308541.5:n.875-130G>A
ENST00000442468.1:c.845-130G>A	ENSP00000387413.1:n.845-130G>A
ENST00000530231.5:c.875-130G>A	ENSP00000433907.1:n.875-130G>A
NM_000506.3:c.875-130G>A	NP_000497.1:n.875-130G>A
NM_000506.4:c.875-130G>A , LRG_551t1:c.875-130G>A	NP_000497.1:n.875-130G>A
NM_001311257.1:c.827-130G>A	NP_001298186.1:n.827-130G>A
XR_428840.2:n.919-130G>A
XR_428840.4:n.910-130G>A
NM_000506.5:c.875-130G>A MANE Select	NP_000497.1:n.875-130G>A
NM_001311257.2:c.827-130G>A	NP_001298186.1:n.827-130G>A