Canonical Allele Identifier: CA1137776760

Gene: F9

Linked Data

• dbSNP Id: rs959637546
• gnomAD v3: X-139550932-AT-A
• gnomAD v4: X-139550932-AT-A

Genomic Alleles

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

Transcript Alleles

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