Canonical Allele Identifier: CA2466828448

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904910A= , CM000685.2:g.154904910A=	GRCh38
NC_000023.10:g.154133185A= , CM000685.1:g.154133185A=	GRCh37
NC_000023.9:g.153786379A=	NCBI36
NG_011403.1:g.122814T=
NG_011403.2:g.122814T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5487T= MANE Select	ENSP00000353393.4:p.Asn1829=
ENST00000360256.8:c.5487T=	ENSP00000353393.4:p.Asn1829=
NM_000132.3:c.5487T=	NP_000123.1:p.Asn1829=
XM_011531126.1:c.5382T=	XP_011529428.1:p.Asn1794=
NM_000132.4:c.5487T= MANE Select	NP_000123.1:p.Asn1829=