Canonical Allele Identifier: CA414913565

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154156881A>T (hg19) ; chrX:g.154928606A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154928606A>T , CM000685.2:g.154928606A>T	GRCh38
NC_000023.10:g.154156881A>T , CM000685.1:g.154156881A>T	GRCh37
NC_000023.9:g.153810075A>T	NCBI36
NG_011403.1:g.99118T>A
NG_011403.2:g.99118T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5184T>A MANE Select	ENSP00000353393.4:p.Tyr1728Ter
ENST00000360256.8:c.5184T>A	ENSP00000353393.4:p.Tyr1728Ter
NM_000132.3:c.5184T>A	NP_000123.1:p.Tyr1728Ter
XM_011531126.1:c.5079T>A	XP_011529428.1:p.Tyr1693Ter
NM_000132.4:c.5184T>A MANE Select	NP_000123.1:p.Tyr1728Ter