Canonical Allele Identifier: CA2466845356

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957097C= , CM000685.2:g.154957097C=	GRCh38
NC_000023.10:g.154185372C= , CM000685.1:g.154185372C=	GRCh37
NC_000023.9:g.153838566C=	NCBI36
NG_011403.1:g.70627G=
NG_011403.2:g.70627G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1612G= MANE Select	ENSP00000353393.4:p.Asp538=
ENST00000647125.1:c.*1488G=	ENSP00000496062.1:n.*1488G=
ENST00000360256.8:c.1612G=	ENSP00000353393.4:p.Asp538=
NM_000132.3:c.1612G=	NP_000123.1:p.Asp538=
XM_011531126.1:c.1507G=	XP_011529428.1:p.Asp503=
NM_000132.4:c.1612G= MANE Select	NP_000123.1:p.Asp538=