Canonical Allele Identifier: CA414910474

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154182194C>A (hg19) ; chrX:g.154953919C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154953919C>A , CM000685.2:g.154953919C>A	GRCh38
NC_000023.10:g.154182194C>A , CM000685.1:g.154182194C>A	GRCh37
NC_000023.9:g.153835388C>A	NCBI36
NG_011403.1:g.73805G>T
NG_011403.2:g.73805G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1876G>T MANE Select	ENSP00000353393.4:p.Glu626Ter
ENST00000647125.1:c.*1752G>T	ENSP00000496062.1:n.*1752G>T
ENST00000360256.8:c.1876G>T	ENSP00000353393.4:p.Glu626Ter
NM_000132.3:c.1876G>T	NP_000123.1:p.Glu626Ter
XM_011531126.1:c.1771G>T	XP_011529428.1:p.Glu591Ter
NM_000132.4:c.1876G>T MANE Select	NP_000123.1:p.Glu626Ter