Canonical Allele Identifier: CA519384162

Gene: F8

Linked Data

• dbSNP Id: rs1365594045
• MyVariant Identifiers: chrX:g.154225354G>A (hg19) ; chrX:g.154997079G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997079G>A , CM000685.2:g.154997079G>A	GRCh38
NC_000023.10:g.154225354G>A , CM000685.1:g.154225354G>A	GRCh37
NC_000023.9:g.153878548G>A	NCBI36
NG_011403.1:g.30645C>T
NG_011403.2:g.30645C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.282C>T MANE Select	ENSP00000353393.4:p.Thr94=
ENST00000647125.1:c.*68C>T	ENSP00000496062.1:n.*68C>T
ENST00000360256.8:c.282C>T	ENSP00000353393.4:p.Thr94=
ENST00000423959.5:c.177C>T	ENSP00000409446.1:p.Thr59=
ENST00000453950.1:c.264C>T	ENSP00000389153.1:p.Thr88=
NM_000132.3:c.282C>T	NP_000123.1:p.Thr94=
XM_011531126.1:c.177C>T	XP_011529428.1:p.Thr59=
NM_000132.4:c.282C>T MANE Select	NP_000123.1:p.Thr94=