Canonical Allele Identifier: CA2466827616
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902046C= , CM000685.2:g.154902046C= GRCh38
NC_000023.10:g.154130321C= , CM000685.1:g.154130321C= GRCh37
NC_000023.9:g.153783515C= NCBI36
NG_011403.1:g.125678G=
NG_011403.2:g.125678G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6115+5G= MANE Select ENSP00000353393.4:n.6115+5G=
ENST00000360256.8:c.6115+5G= ENSP00000353393.4:n.6115+5G=
NM_000132.3:c.6115+5G= NP_000123.1:n.6115+5G=
XM_011531126.1:c.6010+5G= XP_011529428.1:n.6010+5G=
NM_000132.4:c.6115+5G= MANE Select NP_000123.1:n.6115+5G=