Canonical Allele Identifier: CA2466865479

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022638T= , CM000685.2:g.155022638T=	GRCh38
NC_000023.10:g.154250913T= , CM000685.1:g.154250913T=	GRCh37
NC_000023.9:g.153904107T=	NCBI36
NG_011403.1:g.5086A=
NG_011403.2:g.5086A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-86A= MANE Select	ENSP00000353393.4:n.-86A=
ENST00000647125.1:c.-86A=	ENSP00000496062.1:n.-86A=
ENST00000360256.8:c.-86A=	ENSP00000353393.4:n.-86A=
ENST00000423959.5:c.38+4142A=	ENSP00000409446.1:n.38+4142A=
ENST00000453950.1:c.39-142A=	ENSP00000389153.1:n.39-142A=
NM_000132.3:c.-86A=	NP_000123.1:n.-86A=
XM_011531126.1:c.38+4142A=	XP_011529428.1:n.38+4142A=
NM_000132.4:c.-86A= MANE Select	NP_000123.1:n.-86A=