Canonical Allele Identifier: CA519357244

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154133173A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904898A>G , CM000685.2:g.154904898A>G	GRCh38
NC_000023.10:g.154133173A>G , CM000685.1:g.154133173A>G	GRCh37
NC_000023.9:g.153786367A>G	NCBI36
NG_011403.1:g.122826T>C
NG_011403.2:g.122826T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5499T>C MANE Select	ENSP00000353393.4:p.Thr1833=
ENST00000360256.8:c.5499T>C	ENSP00000353393.4:p.Thr1833=
NM_000132.3:c.5499T>C	NP_000123.1:p.Thr1833=
XM_011531126.1:c.5394T>C	XP_011529428.1:p.Thr1798=
NM_000132.4:c.5499T>C MANE Select	NP_000123.1:p.Thr1833=