Canonical Allele Identifier: CA336137330

Gene: F9

Linked Data

• dbSNP Id: rs959637546
• gnomAD v3: X-139550932-A-AT
• gnomAD v4: X-139550932-A-AT
• MyVariant Identifiers: chrX:g.138633091_138633092insT (hg19) ; chrX:g.139550932_139550933insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139550939dup , CM000685.2:g.139550939dup	GRCh38
NC_000023.10:g.138633098dup , CM000685.1:g.138633098dup	GRCh37
NC_000023.9:g.138460764dup	NCBI36
NG_007994.1:g.25204dup , LRG_556:g.25204dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.521-123dup MANE Select	ENSP00000218099.2:n.521-123dup
ENST00000643157.1:n.1188-123dup
ENST00000218099.6:c.521-123dup	ENSP00000218099.2:n.521-123dup
ENST00000394090.2:c.407-123dup	ENSP00000377650.2:n.407-123dup
NM_000133.3:c.521-123dup , LRG_556t1:c.521-123dup	NP_000124.1:n.521-123dup
NM_001313913.1:c.407-123dup	NP_001300842.1:n.407-123dup
XM_005262397.3:c.392-123dup	XP_005262454.1:n.392-123dup
XM_005262397.4:c.392-123dup	XP_005262454.1:n.392-123dup
NM_000133.4:c.521-123dup MANE Select	NP_000124.1:n.521-123dup
NM_001313913.2:c.407-123dup	NP_001300842.1:n.407-123dup