Canonical Allele Identifier: CA2466844342

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154953977G= , CM000685.2:g.154953977G=	GRCh38
NC_000023.10:g.154182252G= , CM000685.1:g.154182252G=	GRCh37
NC_000023.9:g.153835446G=	NCBI36
NG_011403.1:g.73747C=
NG_011403.2:g.73747C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1818C= MANE Select	ENSP00000353393.4:p.Leu606=
ENST00000647125.1:c.*1694C=	ENSP00000496062.1:n.*1694C=
ENST00000360256.8:c.1818C=	ENSP00000353393.4:p.Leu606=
NM_000132.3:c.1818C=	NP_000123.1:p.Leu606=
XM_011531126.1:c.1713C=	XP_011529428.1:p.Leu571=
NM_000132.4:c.1818C= MANE Select	NP_000123.1:p.Leu606=