Canonical Allele Identifier: CA414434506

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139530853G>A , CM000685.2:g.139530853G>A	GRCh38
NC_000023.10:g.138613012G>A , CM000685.1:g.138613012G>A	GRCh37
NC_000023.9:g.138440678G>A	NCBI36
NG_007994.1:g.5118G>A , LRG_556:g.5118G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000133.4:c.88+1G>A MANE Select	NP_000124.1:n.88+1G>A
ENST00000218099.7:c.88+1G>A MANE Select	ENSP00000218099.2:n.88+1G>A
NM_000133.3:c.88+1G>A , LRG_556t1:c.88+1G>A	NP_000124.1:n.88+1G>A
NM_001313913.1:c.88+1G>A	NP_001300842.1:n.88+1G>A
NM_001313913.2:c.88+1G>A	NP_001300842.1:n.88+1G>A
ENST00000218099.6:c.88+1G>A	ENSP00000218099.2:n.88+1G>A
ENST00000394090.2:c.88+1G>A	ENSP00000377650.2:n.88+1G>A
ENST00000479617.2:n.95+1G>A
XM_005262397.3:c.88+1G>A	XP_005262454.1:n.88+1G>A
XM_005262397.4:c.88+1G>A	XP_005262454.1:n.88+1G>A