Canonical Allele Identifier: CA2466835729
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928571C= , CM000685.2:g.154928571C= GRCh38
NC_000023.10:g.154156846C= , CM000685.1:g.154156846C= GRCh37
NC_000023.9:g.153810040C= NCBI36
NG_011403.1:g.99153G=
NG_011403.2:g.99153G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5219G= MANE Select ENSP00000353393.4:p.Arg1740=
ENST00000360256.8:c.5219G= ENSP00000353393.4:p.Arg1740=
NM_000132.3:c.5219G= NP_000123.1:p.Arg1740=
XM_011531126.1:c.5114G= XP_011529428.1:p.Arg1705=
NM_000132.4:c.5219G= MANE Select NP_000123.1:p.Arg1740=