Canonical Allele Identifier: CA519357877

Gene: F8

Linked Data

• COSMIC: COSM3748778 ; COSM3748779
• MyVariant Identifiers: chrX:g.154091413A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863138A>G , CM000685.2:g.154863138A>G	GRCh38
NC_000023.10:g.154091413A>G , CM000685.1:g.154091413A>G	GRCh37
NC_000023.9:g.153744607A>G	NCBI36
NG_011403.1:g.164586T>C
NG_011403.2:g.164586T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6519T>C MANE Select	ENSP00000353393.4:p.Thr2173=
ENST00000644698.1:c.252T>C	ENSP00000495706.1:p.Thr84=
ENST00000330287.10:c.114T>C	ENSP00000327895.6:p.Thr38=
ENST00000360256.8:c.6519T>C	ENSP00000353393.4:p.Thr2173=
NM_000132.3:c.6519T>C	NP_000123.1:p.Thr2173=
NM_019863.2:c.114T>C	NP_063916.1:p.Thr38=
XM_011531126.1:c.6414T>C	XP_011529428.1:p.Thr2138=
NM_000132.4:c.6519T>C MANE Select	NP_000123.1:p.Thr2173=
NM_019863.3:c.114T>C	NP_063916.1:p.Thr38=