Canonical Allele Identifier: CA414914557

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154194296T>A (hg19) ; chrX:g.154966021T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154966021T>A , CM000685.2:g.154966021T>A	GRCh38
NC_000023.10:g.154194296T>A , CM000685.1:g.154194296T>A	GRCh37
NC_000023.9:g.153847490T>A	NCBI36
NG_011403.1:g.61703A>T
NG_011403.2:g.61703A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1392A>T MANE Select	ENSP00000353393.4:p.Glu464Asp
ENST00000647125.1:c.*1268A>T	ENSP00000496062.1:n.*1268A>T
ENST00000360256.8:c.1392A>T	ENSP00000353393.4:p.Glu464Asp
ENST00000483822.2:n.212A>T
NM_000132.3:c.1392A>T	NP_000123.1:p.Glu464Asp
XM_011531126.1:c.1287A>T	XP_011529428.1:p.Glu429Asp
NM_000132.4:c.1392A>T MANE Select	NP_000123.1:p.Glu464Asp