Canonical Allele Identifier: CA2466835728
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928570C= , CM000685.2:g.154928570C= GRCh38
NC_000023.10:g.154156845C= , CM000685.1:g.154156845C= GRCh37
NC_000023.9:g.153810039C= NCBI36
NG_011403.1:g.99154G=
NG_011403.2:g.99154G=

Transcript Alleles

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