Canonical Allele Identifier: CA1969072445

Gene: F2

Linked Data

• dbSNP Id: rs1592412616
• gnomAD v4: 11-46726253-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726253C>T , CM000673.2:g.46726253C>T	GRCh38
NC_000011.9:g.46747803C>T , CM000673.1:g.46747803C>T	GRCh37
NC_000011.8:g.46704379C>T	NCBI36
NG_008953.1:g.12061C>T , LRG_551:g.12061C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+80C>T MANE Select	ENSP00000308541.5:n.874+80C>T
ENST00000311907.9:c.874+80C>T	ENSP00000308541.5:n.874+80C>T
ENST00000442468.1:c.844+80C>T	ENSP00000387413.1:n.844+80C>T
ENST00000530231.5:c.874+80C>T	ENSP00000433907.1:n.874+80C>T
NM_000506.3:c.874+80C>T	NP_000497.1:n.874+80C>T
NM_000506.4:c.874+80C>T , LRG_551t1:c.874+80C>T	NP_000497.1:n.874+80C>T
NM_001311257.1:c.826+80C>T	NP_001298186.1:n.826+80C>T
XR_428840.2:n.918+80C>T
XR_428840.4:n.909+80C>T
NM_000506.5:c.874+80C>T MANE Select	NP_000497.1:n.874+80C>T
NM_001311257.2:c.826+80C>T	NP_001298186.1:n.826+80C>T