Canonical Allele Identifier: CA2613334383

Gene: F2

Linked Data

• gnomAD v4: 11-46725757-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725757C>A , CM000673.2:g.46725757C>A	GRCh38
NC_000011.9:g.46747307C>A , CM000673.1:g.46747307C>A	GRCh37
NC_000011.8:g.46703883C>A	NCBI36
NG_008953.1:g.11565C>A , LRG_551:g.11565C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.560-102C>A MANE Select	ENSP00000308541.5:n.560-102C>A
ENST00000311907.9:c.560-102C>A	ENSP00000308541.5:n.560-102C>A
ENST00000442468.1:c.530-102C>A	ENSP00000387413.1:n.530-102C>A
ENST00000490274.1:n.340-102C>A
ENST00000530231.5:c.560-102C>A	ENSP00000433907.1:n.560-102C>A
NM_000506.3:c.560-102C>A	NP_000497.1:n.560-102C>A
NM_000506.4:c.560-102C>A , LRG_551t1:c.560-102C>A	NP_000497.1:n.560-102C>A
NM_001311257.1:c.512-102C>A	NP_001298186.1:n.512-102C>A
XR_428840.2:n.604-102C>A
XR_428840.4:n.595-102C>A
NM_000506.5:c.560-102C>A MANE Select	NP_000497.1:n.560-102C>A
NM_001311257.2:c.512-102C>A	NP_001298186.1:n.512-102C>A