Canonical Allele Identifier: CA255157
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10268
dbSNP Id: rs137852439

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928647G>C , CM000685.2:g.154928647G>C GRCh38
NC_000023.10:g.154156922G>C , CM000685.1:g.154156922G>C GRCh37
NC_000023.9:g.153810116G>C NCBI36
NG_011403.1:g.99077C>G
NG_011403.2:g.99077C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5143C>G MANE Select ENSP00000353393.4:p.Arg1715Gly
ENST00000360256.8:c.5143C>G ENSP00000353393.4:p.Arg1715Gly
NM_000132.3:c.5143C>G NP_000123.1:p.Arg1715Gly
XM_011531126.1:c.5038C>G XP_011529428.1:p.Arg1680Gly
NM_000132.4:c.5143C>G MANE Select NP_000123.1:p.Arg1715Gly