Canonical Allele Identifier: CA2466856497

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154992947A= , CM000685.2:g.154992947A=	GRCh38
NC_000023.10:g.154221222A= , CM000685.1:g.154221222A=	GRCh37
NC_000023.9:g.153874416A=	NCBI36
NG_011403.1:g.34777T=
NG_011403.2:g.34777T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.590T= MANE Select	ENSP00000353393.4:p.Val197=
ENST00000647125.1:c.*376T=	ENSP00000496062.1:n.*376T=
ENST00000360256.8:c.590T=	ENSP00000353393.4:p.Val197=
ENST00000423959.5:c.485T=	ENSP00000409446.1:p.Val162=
NM_000132.3:c.590T=	NP_000123.1:p.Val197=
XM_011531126.1:c.485T=	XP_011529428.1:p.Val162=
NM_000132.4:c.590T= MANE Select	NP_000123.1:p.Val197=