Canonical Allele Identifier: CA519367632

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154197775G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154969500G>A , CM000685.2:g.154969500G>A	GRCh38
NC_000023.10:g.154197775G>A , CM000685.1:g.154197775G>A	GRCh37
NC_000023.9:g.153850969G>A	NCBI36
NG_011403.1:g.58224C>T
NG_011403.2:g.58224C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.840C>T MANE Select	ENSP00000353393.4:p.Gly280=
ENST00000647125.1:c.*716C>T	ENSP00000496062.1:n.*716C>T
ENST00000360256.8:c.840C>T	ENSP00000353393.4:p.Gly280=
NM_000132.3:c.840C>T	NP_000123.1:p.Gly280=
XM_011531126.1:c.735C>T	XP_011529428.1:p.Gly245=
NM_000132.4:c.840C>T MANE Select	NP_000123.1:p.Gly280=