Canonical Allele Identifier: CA519356212

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154088806T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860531T>G , CM000685.2:g.154860531T>G	GRCh38
NC_000023.10:g.154088806T>G , CM000685.1:g.154088806T>G	GRCh37
NC_000023.9:g.153742000T>G	NCBI36
NG_011403.1:g.167193A>C
NG_011403.2:g.167193A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6801A>C MANE Select	ENSP00000353393.4:p.Val2267=
ENST00000644698.1:c.534A>C	ENSP00000495706.1:p.Val178=
ENST00000330287.10:c.396A>C	ENSP00000327895.6:p.Val132=
ENST00000360256.8:c.6801A>C	ENSP00000353393.4:p.Val2267=
NM_000132.3:c.6801A>C	NP_000123.1:p.Val2267=
NM_019863.2:c.396A>C	NP_063916.1:p.Val132=
XM_011531126.1:c.6696A>C	XP_011529428.1:p.Val2232=
NM_000132.4:c.6801A>C MANE Select	NP_000123.1:p.Val2267=
NM_019863.3:c.396A>C	NP_063916.1:p.Val132=