Canonical Allele Identifier: CA519356063

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154132182T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903907T>G , CM000685.2:g.154903907T>G	GRCh38
NC_000023.10:g.154132182T>G , CM000685.1:g.154132182T>G	GRCh37
NC_000023.9:g.153785376T>G	NCBI36
NG_011403.1:g.123817A>C
NG_011403.2:g.123817A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5997A>C MANE Select	ENSP00000353393.4:p.Pro1999=
ENST00000360256.8:c.5997A>C	ENSP00000353393.4:p.Pro1999=
NM_000132.3:c.5997A>C	NP_000123.1:p.Pro1999=
XM_011531126.1:c.5892A>C	XP_011529428.1:p.Pro1964=
NM_000132.4:c.5997A>C MANE Select	NP_000123.1:p.Pro1999=