Canonical Allele Identifier: CA380264744
Gene: F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725901G>T , CM000673.2:g.46725901G>T GRCh38
NC_000011.9:g.46747451G>T , CM000673.1:g.46747451G>T GRCh37
NC_000011.8:g.46704027G>T NCBI36
NG_008953.1:g.11709G>T , LRG_551:g.11709G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.602G>T MANE Select ENSP00000308541.5:p.Gly201Val
ENST00000311907.9:c.602G>T ENSP00000308541.5:p.Gly201Val
ENST00000442468.1:c.572G>T ENSP00000387413.1:p.Gly191Val
ENST00000490274.1:n.382G>T
ENST00000530231.5:c.602G>T ENSP00000433907.1:p.Gly201Val
NM_000506.3:c.602G>T NP_000497.1:p.Gly201Val
NM_000506.4:c.602G>T , LRG_551t1:c.602G>T NP_000497.1:p.Gly201Val
NM_001311257.1:c.554G>T NP_001298186.1:p.Gly185Val
XR_428840.2:n.646G>T
XR_428840.4:n.637G>T
NM_000506.5:c.602G>T MANE Select NP_000497.1:p.Gly201Val
NM_001311257.2:c.554G>T NP_001298186.1:p.Gly185Val