Canonical Allele Identifier: CA2544641676

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154953861A>T , CM000685.2:g.154953861A>T	GRCh38
NC_000023.10:g.154182136A>T , CM000685.1:g.154182136A>T	GRCh37
NC_000023.9:g.153835330A>T	NCBI36
NG_011403.1:g.73863T>A
NG_011403.2:g.73863T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1903+31T>A MANE Select	ENSP00000353393.4:n.1903+31T>A
ENST00000647125.1:c.*1779+31T>A	ENSP00000496062.1:n.*1779+31T>A
ENST00000360256.8:c.1903+31T>A	ENSP00000353393.4:n.1903+31T>A
NM_000132.3:c.1903+31T>A	NP_000123.1:n.1903+31T>A
XM_011531126.1:c.1798+31T>A	XP_011529428.1:n.1798+31T>A
NM_000132.4:c.1903+31T>A MANE Select	NP_000123.1:n.1903+31T>A