Canonical Allele Identifier: CA2466815638

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863139G= , CM000685.2:g.154863139G=	GRCh38
NC_000023.10:g.154091414G= , CM000685.1:g.154091414G=	GRCh37
NC_000023.9:g.153744608G=	NCBI36
NG_011403.1:g.164585C=
NG_011403.2:g.164585C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6518C= MANE Select	ENSP00000353393.4:p.Thr2173=
ENST00000644698.1:c.251C=	ENSP00000495706.1:p.Thr84=
ENST00000330287.10:c.113C=	ENSP00000327895.6:p.Thr38=
ENST00000360256.8:c.6518C=	ENSP00000353393.4:p.Thr2173=
NM_000132.3:c.6518C=	NP_000123.1:p.Thr2173=
NM_019863.2:c.113C=	NP_063916.1:p.Thr38=
XM_011531126.1:c.6413C=	XP_011529428.1:p.Thr2138=
NM_000132.4:c.6518C= MANE Select	NP_000123.1:p.Thr2173=
NM_019863.3:c.113C=	NP_063916.1:p.Thr38=