Canonical Allele Identifier: CA519357777

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154091359A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863084A>G , CM000685.2:g.154863084A>G	GRCh38
NC_000023.10:g.154091359A>G , CM000685.1:g.154091359A>G	GRCh37
NC_000023.9:g.153744553A>G	NCBI36
NG_011403.1:g.164640T>C
NG_011403.2:g.164640T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6573T>C MANE Select	ENSP00000353393.4:p.Asn2191=
ENST00000644698.1:c.306T>C	ENSP00000495706.1:p.Asn102=
ENST00000330287.10:c.168T>C	ENSP00000327895.6:p.Asn56=
ENST00000360256.8:c.6573T>C	ENSP00000353393.4:p.Asn2191=
NM_000132.3:c.6573T>C	NP_000123.1:p.Asn2191=
NM_019863.2:c.168T>C	NP_063916.1:p.Asn56=
XM_011531126.1:c.6468T>C	XP_011529428.1:p.Asn2156=
NM_000132.4:c.6573T>C MANE Select	NP_000123.1:p.Asn2191=
NM_019863.3:c.168T>C	NP_063916.1:p.Asn56=