Canonical Allele Identifier: CA255124
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10232
dbSNP Id: rs137852424

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953991G>A , CM000685.2:g.154953991G>A GRCh38
NC_000023.10:g.154182266G>A , CM000685.1:g.154182266G>A GRCh37
NC_000023.9:g.153835460G>A NCBI36
NG_011403.1:g.73733C>T
NG_011403.2:g.73733C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1804C>T MANE Select ENSP00000353393.4:p.Arg602Ter
ENST00000647125.1:c.*1680C>T ENSP00000496062.1:n.*1680C>T
ENST00000360256.8:c.1804C>T ENSP00000353393.4:p.Arg602Ter
NM_000132.3:c.1804C>T NP_000123.1:p.Arg602Ter
XM_011531126.1:c.1699C>T XP_011529428.1:p.Arg567Ter
NM_000132.4:c.1804C>T MANE Select NP_000123.1:p.Arg602Ter