Canonical Allele Identifier: CA2466807436

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837673A= , CM000685.2:g.154837673A=	GRCh38
NC_000023.10:g.154065948A= , CM000685.1:g.154065948A=	GRCh37
NC_000023.9:g.153719142A=	NCBI36
NG_011403.1:g.190051T=
NG_033065.1:g.1990T=
NG_011403.2:g.190051T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6980T= MANE Select	ENSP00000353393.4:p.Ile2327=
ENST00000644698.1:c.713T=	ENSP00000495706.1:p.Ile238=
ENST00000330287.10:c.575T=	ENSP00000327895.6:p.Ile192=
ENST00000360256.8:c.6980T=	ENSP00000353393.4:p.Ile2327=
NM_000132.3:c.6980T=	NP_000123.1:p.Ile2327=
NM_019863.2:c.575T=	NP_063916.1:p.Ile192=
XM_011531126.1:c.6875T=	XP_011529428.1:p.Ile2292=
NM_000132.4:c.6980T= MANE Select	NP_000123.1:p.Ile2327=
NM_019863.3:c.575T=	NP_063916.1:p.Ile192=