Canonical Allele Identifier: CA2466814947

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860375C= , CM000685.2:g.154860375C=	GRCh38
NC_000023.10:g.154088650C= , CM000685.1:g.154088650C=	GRCh37
NC_000023.9:g.153741844C=	NCBI36
NG_011403.1:g.167349G=
NG_011403.2:g.167349G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6900+57G= MANE Select	ENSP00000353393.4:n.6900+57G=
ENST00000644698.1:c.633+57G=	ENSP00000495706.1:n.633+57G=
ENST00000330287.10:c.495+57G=	ENSP00000327895.6:n.495+57G=
ENST00000360256.8:c.6900+57G=	ENSP00000353393.4:n.6900+57G=
NM_000132.3:c.6900+57G=	NP_000123.1:n.6900+57G=
NM_019863.2:c.495+57G=	NP_063916.1:n.495+57G=
XM_011531126.1:c.6795+57G=	XP_011529428.1:n.6795+57G=
NM_000132.4:c.6900+57G= MANE Select	NP_000123.1:n.6900+57G=
NM_019863.3:c.495+57G=	NP_063916.1:n.495+57G=