Canonical Allele Identifier: CA2613334888

Gene: F2

Linked Data

• gnomAD v4: 11-46726256-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726256T>G , CM000673.2:g.46726256T>G	GRCh38
NC_000011.9:g.46747806T>G , CM000673.1:g.46747806T>G	GRCh37
NC_000011.8:g.46704382T>G	NCBI36
NG_008953.1:g.12064T>G , LRG_551:g.12064T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+83T>G MANE Select	ENSP00000308541.5:n.874+83T>G
ENST00000311907.9:c.874+83T>G	ENSP00000308541.5:n.874+83T>G
ENST00000442468.1:c.844+83T>G	ENSP00000387413.1:n.844+83T>G
ENST00000530231.5:c.874+83T>G	ENSP00000433907.1:n.874+83T>G
NM_000506.3:c.874+83T>G	NP_000497.1:n.874+83T>G
NM_000506.4:c.874+83T>G , LRG_551t1:c.874+83T>G	NP_000497.1:n.874+83T>G
NM_001311257.1:c.826+83T>G	NP_001298186.1:n.826+83T>G
XR_428840.2:n.918+83T>G
XR_428840.4:n.909+83T>G
NM_000506.5:c.874+83T>G MANE Select	NP_000497.1:n.874+83T>G
NM_001311257.2:c.826+83T>G	NP_001298186.1:n.826+83T>G