Canonical Allele Identifier: CA2466856535

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154993046C= , CM000685.2:g.154993046C=	GRCh38
NC_000023.10:g.154221321C= , CM000685.1:g.154221321C=	GRCh37
NC_000023.9:g.153874515C=	NCBI36
NG_011403.1:g.34678G=
NG_011403.2:g.34678G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.491G= MANE Select	ENSP00000353393.4:p.Gly164=
ENST00000647125.1:c.*277G=	ENSP00000496062.1:n.*277G=
ENST00000360256.8:c.491G=	ENSP00000353393.4:p.Gly164=
ENST00000423959.5:c.386G=	ENSP00000409446.1:p.Gly129=
ENST00000453950.1:c.473G=	ENSP00000389153.1:p.Gly158=
NM_000132.3:c.491G=	NP_000123.1:p.Gly164=
XM_011531126.1:c.386G=	XP_011529428.1:p.Gly129=
NM_000132.4:c.491G= MANE Select	NP_000123.1:p.Gly164=