Canonical Allele Identifier: CA414905198

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154130439A>T (hg19) ; chrX:g.154902164A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154902164A>T , CM000685.2:g.154902164A>T	GRCh38
NC_000023.10:g.154130439A>T , CM000685.1:g.154130439A>T	GRCh37
NC_000023.9:g.153783633A>T	NCBI36
NG_011403.1:g.125560T>A
NG_011403.2:g.125560T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6002T>A MANE Select	ENSP00000353393.4:p.Val2001Asp
ENST00000360256.8:c.6002T>A	ENSP00000353393.4:p.Val2001Asp
NM_000132.3:c.6002T>A	NP_000123.1:p.Val2001Asp
XM_011531126.1:c.5897T>A	XP_011529428.1:p.Val1966Asp
NM_000132.4:c.6002T>A MANE Select	NP_000123.1:p.Val2001Asp