Canonical Allele Identifier: CA2823819735

Gene: F9

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562224C>G , CM000685.2:g.139562224C>G	GRCh38
NC_000023.10:g.138644383C>G , CM000685.1:g.138644383C>G	GRCh37
NC_000023.9:g.138472049C>G	NCBI36
NG_007994.1:g.36489C>G , LRG_556:g.36489C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*153C>G MANE Select	ENSP00000218099.2:n.*153C>G
ENST00000643157.1:n.1723+483C>G
ENST00000218099.6:c.*153C>G	ENSP00000218099.2:n.*153C>G
NM_000133.3:c.*153C>G , LRG_556t1:c.*153C>G	NP_000124.1:n.*153C>G
NM_001313913.1:c.*153C>G	NP_001300842.1:n.*153C>G
XM_005262397.3:c.*153C>G	XP_005262454.1:n.*153C>G
XM_005262397.4:c.*153C>G	XP_005262454.1:n.*153C>G
NM_000133.4:c.*153C>G MANE Select	NP_000124.1:n.*153C>G
NM_001313913.2:c.*153C>G	NP_001300842.1:n.*153C>G