Canonical Allele Identifier: CA414899472

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154124384T>A (hg19) ; chrX:g.154896109T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896109T>A , CM000685.2:g.154896109T>A	GRCh38
NC_000023.10:g.154124384T>A , CM000685.1:g.154124384T>A	GRCh37
NC_000023.9:g.153777578T>A	NCBI36
NG_011403.1:g.131615A>T
NG_011403.2:g.131615A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6397A>T MANE Select	ENSP00000353393.4:p.Thr2133Ser
ENST00000360256.8:c.6397A>T	ENSP00000353393.4:p.Thr2133Ser
NM_000132.3:c.6397A>T	NP_000123.1:p.Thr2133Ser
XM_011531126.1:c.6292A>T	XP_011529428.1:p.Thr2098Ser
NM_000132.4:c.6397A>T MANE Select	NP_000123.1:p.Thr2133Ser