Canonical Allele Identifier: CA519357791

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154182267G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154953992G>A , CM000685.2:g.154953992G>A	GRCh38
NC_000023.10:g.154182267G>A , CM000685.1:g.154182267G>A	GRCh37
NC_000023.9:g.153835461G>A	NCBI36
NG_011403.1:g.73732C>T
NG_011403.2:g.73732C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1803C>T MANE Select	ENSP00000353393.4:p.Asn601=
ENST00000647125.1:c.*1679C>T	ENSP00000496062.1:n.*1679C>T
ENST00000360256.8:c.1803C>T	ENSP00000353393.4:p.Asn601=
NM_000132.3:c.1803C>T	NP_000123.1:p.Asn601=
XM_011531126.1:c.1698C>T	XP_011529428.1:p.Asn566=
NM_000132.4:c.1803C>T MANE Select	NP_000123.1:p.Asn601=