Canonical Allele Identifier: CA519357896

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154091428G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863153G>T , CM000685.2:g.154863153G>T	GRCh38
NC_000023.10:g.154091428G>T , CM000685.1:g.154091428G>T	GRCh37
NC_000023.9:g.153744622G>T	NCBI36
NG_011403.1:g.164571C>A
NG_011403.2:g.164571C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6504C>A MANE Select	ENSP00000353393.4:p.Ile2168=
ENST00000644698.1:c.237C>A	ENSP00000495706.1:p.Ile79=
ENST00000330287.10:c.99C>A	ENSP00000327895.6:p.Ile33=
ENST00000360256.8:c.6504C>A	ENSP00000353393.4:p.Ile2168=
NM_000132.3:c.6504C>A	NP_000123.1:p.Ile2168=
NM_019863.2:c.99C>A	NP_063916.1:p.Ile33=
XM_011531126.1:c.6399C>A	XP_011529428.1:p.Ile2133=
NM_000132.4:c.6504C>A MANE Select	NP_000123.1:p.Ile2168=
NM_019863.3:c.99C>A	NP_063916.1:p.Ile33=