Canonical Allele Identifier: CA2613334378
Gene: F2 HGNC NCBI

Linked Data

gnomAD v4: 11-46725749-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725749C>A , CM000673.2:g.46725749C>A GRCh38
NC_000011.9:g.46747299C>A , CM000673.1:g.46747299C>A GRCh37
NC_000011.8:g.46703875C>A NCBI36
NG_008953.1:g.11557C>A , LRG_551:g.11557C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.560-110C>A MANE Select ENSP00000308541.5:n.560-110C>A
ENST00000311907.9:c.560-110C>A ENSP00000308541.5:n.560-110C>A
ENST00000442468.1:c.530-110C>A ENSP00000387413.1:n.530-110C>A
ENST00000490274.1:n.340-110C>A
ENST00000530231.5:c.560-110C>A ENSP00000433907.1:n.560-110C>A
NM_000506.3:c.560-110C>A NP_000497.1:n.560-110C>A
NM_000506.4:c.560-110C>A , LRG_551t1:c.560-110C>A NP_000497.1:n.560-110C>A
NM_001311257.1:c.512-110C>A NP_001298186.1:n.512-110C>A
XR_428840.2:n.604-110C>A
XR_428840.4:n.595-110C>A
NM_000506.5:c.560-110C>A MANE Select NP_000497.1:n.560-110C>A
NM_001311257.2:c.512-110C>A NP_001298186.1:n.512-110C>A
Search 100 bp 5'
Search 100 bp 3'