Canonical Allele Identifier: CA2466815550

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863039C= , CM000685.2:g.154863039C=	GRCh38
NC_000023.10:g.154091314C= , CM000685.1:g.154091314C=	GRCh37
NC_000023.9:g.153744508C=	NCBI36
NG_011403.1:g.164685G=
NG_011403.2:g.164685G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6574+44G= MANE Select	ENSP00000353393.4:n.6574+44G=
ENST00000644698.1:c.307+44G=	ENSP00000495706.1:n.307+44G=
ENST00000330287.10:c.169+44G=	ENSP00000327895.6:n.169+44G=
ENST00000360256.8:c.6574+44G=	ENSP00000353393.4:n.6574+44G=
NM_000132.3:c.6574+44G=	NP_000123.1:n.6574+44G=
NM_019863.2:c.169+44G=	NP_063916.1:n.169+44G=
XM_011531126.1:c.6469+44G=	XP_011529428.1:n.6469+44G=
NM_000132.4:c.6574+44G= MANE Select	NP_000123.1:n.6574+44G=
NM_019863.3:c.169+44G=	NP_063916.1:n.169+44G=