Canonical Allele Identifier: CA414908674

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154133167A>T (hg19) ; chrX:g.154904892A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904892A>T , CM000685.2:g.154904892A>T	GRCh38
NC_000023.10:g.154133167A>T , CM000685.1:g.154133167A>T	GRCh37
NC_000023.9:g.153786361A>T	NCBI36
NG_011403.1:g.122832T>A
NG_011403.2:g.122832T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5505T>A MANE Select	ENSP00000353393.4:p.Phe1835Leu
ENST00000360256.8:c.5505T>A	ENSP00000353393.4:p.Phe1835Leu
NM_000132.3:c.5505T>A	NP_000123.1:p.Phe1835Leu
XM_011531126.1:c.5400T>A	XP_011529428.1:p.Phe1800Leu
NM_000132.4:c.5505T>A MANE Select	NP_000123.1:p.Phe1835Leu