Canonical Allele Identifier: CA380264885
Gene: F2 HGNC NCBI

Linked Data

dbSNP Id: rs1165489725

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46725940T>C , CM000673.2:g.46725940T>C GRCh38
NC_000011.9:g.46747490T>C , CM000673.1:g.46747490T>C GRCh37
NC_000011.8:g.46704066T>C NCBI36
NG_008953.1:g.11748T>C , LRG_551:g.11748T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.641T>C MANE Select ENSP00000308541.5:p.Val214Ala
ENST00000311907.9:c.641T>C ENSP00000308541.5:p.Val214Ala
ENST00000442468.1:c.611T>C ENSP00000387413.1:p.Val204Ala
ENST00000490274.1:n.421T>C
ENST00000530231.5:c.641T>C ENSP00000433907.1:p.Val214Ala
NM_000506.3:c.641T>C NP_000497.1:p.Val214Ala
NM_000506.4:c.641T>C , LRG_551t1:c.641T>C NP_000497.1:p.Val214Ala
NM_001311257.1:c.593T>C NP_001298186.1:p.Val198Ala
XR_428840.2:n.685T>C
XR_428840.4:n.676T>C
NM_000506.5:c.641T>C MANE Select NP_000497.1:p.Val214Ala
NM_001311257.2:c.593T>C NP_001298186.1:p.Val198Ala