Canonical Allele Identifier: CA519717957

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154132329G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904054G>A , CM000685.2:g.154904054G>A	GRCh38
NC_000023.10:g.154132329G>A , CM000685.1:g.154132329G>A	GRCh37
NC_000023.9:g.153785523G>A	NCBI36
NG_011403.1:g.123670C>T
NG_011403.2:g.123670C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5850C>T MANE Select	ENSP00000353393.4:p.Gly1950=
ENST00000360256.8:c.5850C>T	ENSP00000353393.4:p.Gly1950=
NM_000132.3:c.5850C>T	NP_000123.1:p.Gly1950=
XM_011531126.1:c.5745C>T	XP_011529428.1:p.Gly1915=
NM_000132.4:c.5850C>T MANE Select	NP_000123.1:p.Gly1950=