Canonical Allele Identifier: CA380269507
Gene: F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46728058A>C , CM000673.2:g.46728058A>C GRCh38
NC_000011.9:g.46749608A>C , CM000673.1:g.46749608A>C GRCh37
NC_000011.8:g.46706184A>C NCBI36
NG_008953.1:g.13866A>C , LRG_551:g.13866A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.1193A>C MANE Select ENSP00000308541.5:p.Asp398Ala
ENST00000311907.9:c.1193A>C ENSP00000308541.5:p.Asp398Ala
ENST00000530231.5:c.1193A>C ENSP00000433907.1:p.Asp398Ala
NM_000506.3:c.1193A>C NP_000497.1:p.Asp398Ala
NM_000506.4:c.1193A>C , LRG_551t1:c.1193A>C NP_000497.1:p.Asp398Ala
NM_001311257.1:c.1145A>C NP_001298186.1:p.Asp382Ala
XR_428840.2:n.1237A>C
XR_428840.4:n.1228A>C
NM_000506.5:c.1193A>C MANE Select NP_000497.1:p.Asp398Ala
NM_001311257.2:c.1145A>C NP_001298186.1:p.Asp382Ala