Canonical Allele Identifier: CA2841394531

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537194C>G , CM000685.2:g.139537194C>G	GRCh38
NC_000023.10:g.138619353C>G , CM000685.1:g.138619353C>G	GRCh37
NC_000023.9:g.138447019C>G	NCBI36
NG_007994.1:g.11459C>G , LRG_556:g.11459C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.252+21C>G MANE Select	ENSP00000218099.2:n.252+21C>G
ENST00000218099.6:c.252+21C>G	ENSP00000218099.2:n.252+21C>G
ENST00000394090.2:c.252+21C>G	ENSP00000377650.2:n.252+21C>G
ENST00000479617.2:n.241+39C>G
NM_000133.3:c.252+21C>G , LRG_556t1:c.252+21C>G	NP_000124.1:n.252+21C>G
NM_001313913.1:c.252+21C>G	NP_001300842.1:n.252+21C>G
XM_005262397.3:c.252+21C>G	XP_005262454.1:n.252+21C>G
XM_005262397.4:c.252+21C>G	XP_005262454.1:n.252+21C>G
NM_000133.4:c.252+21C>G MANE Select	NP_000124.1:n.252+21C>G
NM_001313913.2:c.252+21C>G	NP_001300842.1:n.252+21C>G