Canonical Allele Identifier: CA2466835821
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928836C= , CM000685.2:g.154928836C= GRCh38
NC_000023.10:g.154157111C= , CM000685.1:g.154157111C= GRCh37
NC_000023.9:g.153810305C= NCBI36
NG_011403.1:g.98888G=
NG_011403.2:g.98888G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4954G= MANE Select ENSP00000353393.4:p.Glu1652=
ENST00000360256.8:c.4954G= ENSP00000353393.4:p.Glu1652=
NM_000132.3:c.4954G= NP_000123.1:p.Glu1652=
XM_011531126.1:c.4849G= XP_011529428.1:p.Glu1617=
NM_000132.4:c.4954G= MANE Select NP_000123.1:p.Glu1652=