Canonical Allele Identifier: CA414908495

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154133117T>A (hg19) ; chrX:g.154904842T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904842T>A , CM000685.2:g.154904842T>A	GRCh38
NC_000023.10:g.154133117T>A , CM000685.1:g.154133117T>A	GRCh37
NC_000023.9:g.153786311T>A	NCBI36
NG_011403.1:g.122882A>T
NG_011403.2:g.122882A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5555A>T MANE Select	ENSP00000353393.4:p.Lys1852Ile
ENST00000360256.8:c.5555A>T	ENSP00000353393.4:p.Lys1852Ile
NM_000132.3:c.5555A>T	NP_000123.1:p.Lys1852Ile
XM_011531126.1:c.5450A>T	XP_011529428.1:p.Lys1817Ile
NM_000132.4:c.5555A>T MANE Select	NP_000123.1:p.Lys1852Ile