Canonical Allele Identifier: CA2466844312

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154953897A= , CM000685.2:g.154953897A=	GRCh38
NC_000023.10:g.154182172A= , CM000685.1:g.154182172A=	GRCh37
NC_000023.9:g.153835366A=	NCBI36
NG_011403.1:g.73827T=
NG_011403.2:g.73827T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1898T= MANE Select	ENSP00000353393.4:p.Met633=
ENST00000647125.1:c.*1774T=	ENSP00000496062.1:n.*1774T=
ENST00000360256.8:c.1898T=	ENSP00000353393.4:p.Met633=
NM_000132.3:c.1898T=	NP_000123.1:p.Met633=
XM_011531126.1:c.1793T=	XP_011529428.1:p.Met598=
NM_000132.4:c.1898T= MANE Select	NP_000123.1:p.Met633=