Canonical Allele Identifier: CA1969071832

Gene: F2

Linked Data

• dbSNP Id: rs2064867831
• gnomAD v4: 11-46725816-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725816T>G , CM000673.2:g.46725816T>G	GRCh38
NC_000011.9:g.46747366T>G , CM000673.1:g.46747366T>G	GRCh37
NC_000011.8:g.46703942T>G	NCBI36
NG_008953.1:g.11624T>G , LRG_551:g.11624T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.560-43T>G MANE Select	ENSP00000308541.5:n.560-43T>G
ENST00000311907.9:c.560-43T>G	ENSP00000308541.5:n.560-43T>G
ENST00000442468.1:c.530-43T>G	ENSP00000387413.1:n.530-43T>G
ENST00000490274.1:n.340-43T>G
ENST00000530231.5:c.560-43T>G	ENSP00000433907.1:n.560-43T>G
NM_000506.3:c.560-43T>G	NP_000497.1:n.560-43T>G
NM_000506.4:c.560-43T>G , LRG_551t1:c.560-43T>G	NP_000497.1:n.560-43T>G
NM_001311257.1:c.512-43T>G	NP_001298186.1:n.512-43T>G
XR_428840.2:n.604-43T>G
XR_428840.4:n.595-43T>G
NM_000506.5:c.560-43T>G MANE Select	NP_000497.1:n.560-43T>G
NM_001311257.2:c.512-43T>G	NP_001298186.1:n.512-43T>G