Canonical Allele Identifier: CA380264739
Gene: F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725900G>T , CM000673.2:g.46725900G>T GRCh38
NC_000011.9:g.46747450G>T , CM000673.1:g.46747450G>T GRCh37
NC_000011.8:g.46704026G>T NCBI36
NG_008953.1:g.11708G>T , LRG_551:g.11708G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.601G>T MANE Select ENSP00000308541.5:p.Gly201Cys
ENST00000311907.9:c.601G>T ENSP00000308541.5:p.Gly201Cys
ENST00000442468.1:c.571G>T ENSP00000387413.1:p.Gly191Cys
ENST00000490274.1:n.381G>T
ENST00000530231.5:c.601G>T ENSP00000433907.1:p.Gly201Cys
NM_000506.3:c.601G>T NP_000497.1:p.Gly201Cys
NM_000506.4:c.601G>T , LRG_551t1:c.601G>T NP_000497.1:p.Gly201Cys
NM_001311257.1:c.553G>T NP_001298186.1:p.Gly185Cys
XR_428840.2:n.645G>T
XR_428840.4:n.636G>T
NM_000506.5:c.601G>T MANE Select NP_000497.1:p.Gly201Cys
NM_001311257.2:c.553G>T NP_001298186.1:p.Gly185Cys