Canonical Allele Identifier: CA2466844374
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154954054A= , CM000685.2:g.154954054A= GRCh38
NC_000023.10:g.154182329A= , CM000685.1:g.154182329A= GRCh37
NC_000023.9:g.153835523A= NCBI36
NG_011403.1:g.73670T=
NG_011403.2:g.73670T=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1753-12T= MANE Select ENSP00000353393.4:n.1753-12T=
ENST00000647125.1:c.*1629-12T= ENSP00000496062.1:n.*1629-12T=
ENST00000360256.8:c.1753-12T= ENSP00000353393.4:n.1753-12T=
NM_000132.3:c.1753-12T= NP_000123.1:n.1753-12T=
XM_011531126.1:c.1648-12T= XP_011529428.1:n.1648-12T=
NM_000132.4:c.1753-12T= MANE Select NP_000123.1:n.1753-12T=