Canonical Allele Identifier: CA519357988

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154091470T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863195T>A , CM000685.2:g.154863195T>A	GRCh38
NC_000023.10:g.154091470T>A , CM000685.1:g.154091470T>A	GRCh37
NC_000023.9:g.153744664T>A	NCBI36
NG_011403.1:g.164529A>T
NG_011403.2:g.164529A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6462A>T MANE Select	ENSP00000353393.4:p.Ile2154=
ENST00000644698.1:c.195A>T	ENSP00000495706.1:p.Ile65=
ENST00000330287.10:c.57A>T	ENSP00000327895.6:p.Ile19=
ENST00000360256.8:c.6462A>T	ENSP00000353393.4:p.Ile2154=
NM_000132.3:c.6462A>T	NP_000123.1:p.Ile2154=
NM_019863.2:c.57A>T	NP_063916.1:p.Ile19=
XM_011531126.1:c.6357A>T	XP_011529428.1:p.Ile2119=
NM_000132.4:c.6462A>T MANE Select	NP_000123.1:p.Ile2154=
NM_019863.3:c.57A>T	NP_063916.1:p.Ile19=