Canonical Allele Identifier: CA519388683

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154250750C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022475C>T , CM000685.2:g.155022475C>T	GRCh38
NC_000023.10:g.154250750C>T , CM000685.1:g.154250750C>T	GRCh37
NC_000023.9:g.153903944C>T	NCBI36
NG_011403.1:g.5249G>A
NG_011403.2:g.5249G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.78G>A MANE Select	ENSP00000353393.4:p.Leu26=
ENST00000647125.1:c.78G>A	ENSP00000496062.1:p.Leu26=
ENST00000360256.8:c.78G>A	ENSP00000353393.4:p.Leu26=
ENST00000423959.5:c.38+4305G>A	ENSP00000409446.1:n.38+4305G>A
ENST00000453950.1:c.60G>A	ENSP00000389153.1:p.Leu20=
NM_000132.3:c.78G>A	NP_000123.1:p.Leu26=
XM_011531126.1:c.38+4305G>A	XP_011529428.1:n.38+4305G>A
NM_000132.4:c.78G>A MANE Select	NP_000123.1:p.Leu26=