Canonical Allele Identifier: CA519355287

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154065980T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837705T>A , CM000685.2:g.154837705T>A	GRCh38
NC_000023.10:g.154065980T>A , CM000685.1:g.154065980T>A	GRCh37
NC_000023.9:g.153719174T>A	NCBI36
NG_011403.1:g.190019A>T
NG_033065.1:g.1958A>T
NG_011403.2:g.190019A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6948A>T MANE Select	ENSP00000353393.4:p.Leu2316=
ENST00000644698.1:c.681A>T	ENSP00000495706.1:p.Leu227=
ENST00000330287.10:c.543A>T	ENSP00000327895.6:p.Leu181=
ENST00000360256.8:c.6948A>T	ENSP00000353393.4:p.Leu2316=
NM_000132.3:c.6948A>T	NP_000123.1:p.Leu2316=
NM_019863.2:c.543A>T	NP_063916.1:p.Leu181=
XM_011531126.1:c.6843A>T	XP_011529428.1:p.Leu2281=
NM_000132.4:c.6948A>T MANE Select	NP_000123.1:p.Leu2316=
NM_019863.3:c.543A>T	NP_063916.1:p.Leu181=