Canonical Allele Identifier: CA1969071745
Gene: F2 HGNC NCBI

Linked Data

dbSNP Id: rs1349702997
gnomAD v4: 11-46725722-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725722G>A , CM000673.2:g.46725722G>A GRCh38
NC_000011.9:g.46747272G>A , CM000673.1:g.46747272G>A GRCh37
NC_000011.8:g.46703848G>A NCBI36
NG_008953.1:g.11530G>A , LRG_551:g.11530G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.560-137G>A MANE Select ENSP00000308541.5:n.560-137G>A
ENST00000311907.9:c.560-137G>A ENSP00000308541.5:n.560-137G>A
ENST00000442468.1:c.530-137G>A ENSP00000387413.1:n.530-137G>A
ENST00000490274.1:n.340-137G>A
ENST00000530231.5:c.560-137G>A ENSP00000433907.1:n.560-137G>A
NM_000506.3:c.560-137G>A NP_000497.1:n.560-137G>A
NM_000506.4:c.560-137G>A , LRG_551t1:c.560-137G>A NP_000497.1:n.560-137G>A
NM_001311257.1:c.512-137G>A NP_001298186.1:n.512-137G>A
XR_428840.2:n.604-137G>A
XR_428840.4:n.595-137G>A
NM_000506.5:c.560-137G>A MANE Select NP_000497.1:n.560-137G>A
NM_001311257.2:c.512-137G>A NP_001298186.1:n.512-137G>A
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