Canonical Allele Identifier: CA2466857821
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997131G= , CM000685.2:g.154997131G= GRCh38
NC_000023.10:g.154225406G= , CM000685.1:g.154225406G= GRCh37
NC_000023.9:g.153878600G= NCBI36
NG_011403.1:g.30593C=
NG_011403.2:g.30593C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.266-36C= MANE Select ENSP00000353393.4:n.266-36C=
ENST00000647125.1:c.*52-36C= ENSP00000496062.1:n.*52-36C=
ENST00000360256.8:c.266-36C= ENSP00000353393.4:n.266-36C=
ENST00000423959.5:c.161-36C= ENSP00000409446.1:n.161-36C=
ENST00000453950.1:c.248-36C= ENSP00000389153.1:n.248-36C=
NM_000132.3:c.266-36C= NP_000123.1:n.266-36C=
XM_011531126.1:c.161-36C= XP_011529428.1:n.161-36C=
NM_000132.4:c.266-36C= MANE Select NP_000123.1:n.266-36C=