Canonical Allele Identifier: CA2466836664
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154931360C= , CM000685.2:g.154931360C= GRCh38
NC_000023.10:g.154159635C= , CM000685.1:g.154159635C= GRCh37
NC_000023.9:g.153812829C= NCBI36
NG_011403.1:g.96364G=
NG_011403.2:g.96364G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.2430G= MANE Select ENSP00000353393.4:p.Leu810=
ENST00000647125.1:c.*2096G= ENSP00000496062.1:n.*2096G=
ENST00000360256.8:c.2430G= ENSP00000353393.4:p.Leu810=
NM_000132.3:c.2430G= NP_000123.1:p.Leu810=
XM_011531126.1:c.2325G= XP_011529428.1:p.Leu775=
NM_000132.4:c.2430G= MANE Select NP_000123.1:p.Leu810=