Canonical Allele Identifier: CA255178
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10289
ClinVar RCV Id: RCV000011002
dbSNP Id: rs28933680

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904493G>C , CM000685.2:g.154904493G>C GRCh38
NC_000023.10:g.154132768G>C , CM000685.1:g.154132768G>C GRCh37
NC_000023.9:g.153785962G>C NCBI36
NG_011403.1:g.123231C>G
NG_011403.2:g.123231C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5618C>G MANE Select ENSP00000353393.4:p.Pro1873Arg
ENST00000360256.8:c.5618C>G ENSP00000353393.4:p.Pro1873Arg
NM_000132.3:c.5618C>G NP_000123.1:p.Pro1873Arg
XM_011531126.1:c.5513C>G XP_011529428.1:p.Pro1838Arg
NM_000132.4:c.5618C>G MANE Select NP_000123.1:p.Pro1873Arg