Canonical Allele Identifier: CA2466835683
Gene: F8 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928432T= , CM000685.2:g.154928432T= GRCh38
NC_000023.10:g.154156707T= , CM000685.1:g.154156707T= GRCh37
NC_000023.9:g.153809901T= NCBI36
NG_011403.1:g.99292A=
NG_011403.2:g.99292A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5219+139A= MANE Select ENSP00000353393.4:n.5219+139A=
ENST00000360256.8:c.5219+139A= ENSP00000353393.4:n.5219+139A=
NM_000132.3:c.5219+139A= NP_000123.1:n.5219+139A=
XM_011531126.1:c.5114+139A= XP_011529428.1:n.5114+139A=
NM_000132.4:c.5219+139A= MANE Select NP_000123.1:n.5219+139A=
Search 100 bp 5'
Search 100 bp 3'