Canonical Allele Identifier: CA519389042

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154250819T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022544T>A , CM000685.2:g.155022544T>A	GRCh38
NC_000023.10:g.154250819T>A , CM000685.1:g.154250819T>A	GRCh37
NC_000023.9:g.153904013T>A	NCBI36
NG_011403.1:g.5180A>T
NG_011403.2:g.5180A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.9A>T MANE Select	ENSP00000353393.4:p.Ile3=
ENST00000647125.1:c.9A>T	ENSP00000496062.1:p.Ile3=
ENST00000360256.8:c.9A>T	ENSP00000353393.4:p.Ile3=
ENST00000423959.5:c.38+4236A>T	ENSP00000409446.1:n.38+4236A>T
ENST00000453950.1:c.39-48A>T	ENSP00000389153.1:n.39-48A>T
NM_000132.3:c.9A>T	NP_000123.1:p.Ile3=
XM_011531126.1:c.38+4236A>T	XP_011529428.1:n.38+4236A>T
NM_000132.4:c.9A>T MANE Select	NP_000123.1:p.Ile3=