Canonical Allele Identifier: CA519355178

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154065896G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837621G>T , CM000685.2:g.154837621G>T	GRCh38
NC_000023.10:g.154065896G>T , CM000685.1:g.154065896G>T	GRCh37
NC_000023.9:g.153719090G>T	NCBI36
NG_011403.1:g.190103C>A
NG_033065.1:g.2042C>A
NG_011403.2:g.190103C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.7032C>A MANE Select	ENSP00000353393.4:p.Gly2344=
ENST00000644698.1:c.765C>A	ENSP00000495706.1:p.Gly255=
ENST00000330287.10:c.627C>A	ENSP00000327895.6:p.Gly209=
ENST00000360256.8:c.7032C>A	ENSP00000353393.4:p.Gly2344=
NM_000132.3:c.7032C>A	NP_000123.1:p.Gly2344=
NM_019863.2:c.627C>A	NP_063916.1:p.Gly209=
XM_011531126.1:c.6927C>A	XP_011529428.1:p.Gly2309=
NM_000132.4:c.7032C>A MANE Select	NP_000123.1:p.Gly2344=
NM_019863.3:c.627C>A	NP_063916.1:p.Gly209=