Canonical Allele Identifier: CA414914217
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928751T>G , CM000685.2:g.154928751T>G GRCh38
NC_000023.10:g.154157026T>G , CM000685.1:g.154157026T>G GRCh37
NC_000023.9:g.153810220T>G NCBI36
NG_011403.1:g.98973A>C
NG_011403.2:g.98973A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5039A>C MANE Select ENSP00000353393.4:p.Glu1680Ala
ENST00000360256.8:c.5039A>C ENSP00000353393.4:p.Glu1680Ala
NM_000132.3:c.5039A>C NP_000123.1:p.Glu1680Ala
XM_011531126.1:c.4934A>C XP_011529428.1:p.Glu1645Ala
NM_000132.4:c.5039A>C MANE Select NP_000123.1:p.Glu1680Ala