Canonical Allele Identifier: CA2466844362

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154954013C= , CM000685.2:g.154954013C=	GRCh38
NC_000023.10:g.154182288C= , CM000685.1:g.154182288C=	GRCh37
NC_000023.9:g.153835482C=	NCBI36
NG_011403.1:g.73711G=
NG_011403.2:g.73711G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1782G= MANE Select	ENSP00000353393.4:p.Leu594=
ENST00000647125.1:c.*1658G=	ENSP00000496062.1:n.*1658G=
ENST00000360256.8:c.1782G=	ENSP00000353393.4:p.Leu594=
NM_000132.3:c.1782G=	NP_000123.1:p.Leu594=
XM_011531126.1:c.1677G=	XP_011529428.1:p.Leu559=
NM_000132.4:c.1782G= MANE Select	NP_000123.1:p.Leu594=