Canonical Allele Identifier: CA519357995

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154091473C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863198C>A , CM000685.2:g.154863198C>A	GRCh38
NC_000023.10:g.154091473C>A , CM000685.1:g.154091473C>A	GRCh37
NC_000023.9:g.153744667C>A	NCBI36
NG_011403.1:g.164526G>T
NG_011403.2:g.164526G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6459G>T MANE Select	ENSP00000353393.4:p.Gly2153=
ENST00000644698.1:c.192G>T	ENSP00000495706.1:p.Gly64=
ENST00000330287.10:c.54G>T	ENSP00000327895.6:p.Gly18=
ENST00000360256.8:c.6459G>T	ENSP00000353393.4:p.Gly2153=
NM_000132.3:c.6459G>T	NP_000123.1:p.Gly2153=
NM_019863.2:c.54G>T	NP_063916.1:p.Gly18=
XM_011531126.1:c.6354G>T	XP_011529428.1:p.Gly2118=
NM_000132.4:c.6459G>T MANE Select	NP_000123.1:p.Gly2153=
NM_019863.3:c.54G>T	NP_063916.1:p.Gly18=