Canonical Allele Identifier: CA380267269

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46748259A>G (hg19) ; chr11:g.46726709A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726709A>G , CM000673.2:g.46726709A>G	GRCh38
NC_000011.9:g.46748259A>G , CM000673.1:g.46748259A>G	GRCh37
NC_000011.8:g.46704835A>G	NCBI36
NG_008953.1:g.12517A>G , LRG_551:g.12517A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1004-2A>G MANE Select	ENSP00000308541.5:n.1004-2A>G
ENST00000311907.9:c.1004-2A>G	ENSP00000308541.5:n.1004-2A>G
ENST00000530231.5:c.1004-2A>G	ENSP00000433907.1:n.1004-2A>G
NM_000506.3:c.1004-2A>G	NP_000497.1:n.1004-2A>G
NM_000506.4:c.1004-2A>G , LRG_551t1:c.1004-2A>G	NP_000497.1:n.1004-2A>G
NM_001311257.1:c.956-2A>G	NP_001298186.1:n.956-2A>G
XR_428840.2:n.1048-2A>G
XR_428840.4:n.1039-2A>G
NM_000506.5:c.1004-2A>G MANE Select	NP_000497.1:n.1004-2A>G
NM_001311257.2:c.956-2A>G	NP_001298186.1:n.956-2A>G