Canonical Allele Identifier: CA2466848135

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154966575C= , CM000685.2:g.154966575C=	GRCh38
NC_000023.10:g.154194850C= , CM000685.1:g.154194850C=	GRCh37
NC_000023.9:g.153848044C=	NCBI36
NG_011403.1:g.61149G=
NG_011403.2:g.61149G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.1122G= MANE Select	ENSP00000353393.4:p.Met374=
ENST00000647125.1:c.*998G=	ENSP00000496062.1:n.*998G=
ENST00000360256.8:c.1122G=	ENSP00000353393.4:p.Met374=
NM_000132.3:c.1122G=	NP_000123.1:p.Met374=
XM_011531126.1:c.1017G=	XP_011529428.1:p.Met339=
NM_000132.4:c.1122G= MANE Select	NP_000123.1:p.Met374=