Canonical Allele Identifier: CA255188
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10297
ClinVar RCV Id: RCV000011010
dbSNP Id: rs111033615

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904004C>T , CM000685.2:g.154904004C>T GRCh38
NC_000023.10:g.154132279C>T , CM000685.1:g.154132279C>T GRCh37
NC_000023.9:g.153785473C>T NCBI36
NG_011403.1:g.123720G>A
NG_011403.2:g.123720G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5900G>A MANE Select ENSP00000353393.4:p.Gly1967Asp
ENST00000360256.8:c.5900G>A ENSP00000353393.4:p.Gly1967Asp
NM_000132.3:c.5900G>A NP_000123.1:p.Gly1967Asp
XM_011531126.1:c.5795G>A XP_011529428.1:p.Gly1932Asp
NM_000132.4:c.5900G>A MANE Select NP_000123.1:p.Gly1967Asp