Canonical Allele Identifier: CA519357160

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154133158C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904883C>A , CM000685.2:g.154904883C>A	GRCh38
NC_000023.10:g.154133158C>A , CM000685.1:g.154133158C>A	GRCh37
NC_000023.9:g.153786352C>A	NCBI36
NG_011403.1:g.122841G>T
NG_011403.2:g.122841G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5514G>T MANE Select	ENSP00000353393.4:p.Val1838=
ENST00000360256.8:c.5514G>T	ENSP00000353393.4:p.Val1838=
NM_000132.3:c.5514G>T	NP_000123.1:p.Val1838=
XM_011531126.1:c.5409G>T	XP_011529428.1:p.Val1803=
NM_000132.4:c.5514G>T MANE Select	NP_000123.1:p.Val1838=