Canonical Allele Identifier: CA2466828453

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904925G= , CM000685.2:g.154904925G=	GRCh38
NC_000023.10:g.154133200G= , CM000685.1:g.154133200G=	GRCh37
NC_000023.9:g.153786394G=	NCBI36
NG_011403.1:g.122799C=
NG_011403.2:g.122799C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5472C= MANE Select	ENSP00000353393.4:p.Asn1824=
ENST00000360256.8:c.5472C=	ENSP00000353393.4:p.Asn1824=
NM_000132.3:c.5472C=	NP_000123.1:p.Asn1824=
XM_011531126.1:c.5367C=	XP_011529428.1:p.Asn1789=
NM_000132.4:c.5472C= MANE Select	NP_000123.1:p.Asn1824=