Canonical Allele Identifier: CA645614542

Gene: F8

Linked Data

• COSMIC: COSM5938484 ; COSM5938485

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903901C>T , CM000685.2:g.154903901C>T	GRCh38
NC_000023.10:g.154132176C>T , CM000685.1:g.154132176C>T	GRCh37
NC_000023.9:g.153785370C>T	NCBI36
NG_011403.1:g.123823G>A
NG_011403.2:g.123823G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5998+5G>A MANE Select	ENSP00000353393.4:n.5998+5G>A
ENST00000360256.8:c.5998+5G>A	ENSP00000353393.4:n.5998+5G>A
NM_000132.3:c.5998+5G>A	NP_000123.1:n.5998+5G>A
XM_011531126.1:c.5893+5G>A	XP_011529428.1:n.5893+5G>A
NM_000132.4:c.5998+5G>A MANE Select	NP_000123.1:n.5998+5G>A