Canonical Allele Identifier: CA414910228

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154182168G>T (hg19) ; chrX:g.154953893G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154953893G>T , CM000685.2:g.154953893G>T	GRCh38
NC_000023.10:g.154182168G>T , CM000685.1:g.154182168G>T	GRCh37
NC_000023.9:g.153835362G>T	NCBI36
NG_011403.1:g.73831C>A
NG_011403.2:g.73831C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1902C>A MANE Select	ENSP00000353393.4:p.His634Gln
ENST00000647125.1:c.*1778C>A	ENSP00000496062.1:n.*1778C>A
ENST00000360256.8:c.1902C>A	ENSP00000353393.4:p.His634Gln
NM_000132.3:c.1902C>A	NP_000123.1:p.His634Gln
XM_011531126.1:c.1797C>A	XP_011529428.1:p.His599Gln
NM_000132.4:c.1902C>A MANE Select	NP_000123.1:p.His634Gln