Canonical Allele Identifier: CA519357895

Gene: F8

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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