Canonical Allele Identifier: CA915952348
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 627496
ClinVar RCV Id: RCV000852257
dbSNP Id: rs1603265760

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139551027_139551348del , CM000685.2:g.139551027_139551348del GRCh38
NC_000023.10:g.138633186_138633507del , CM000685.1:g.138633186_138633507del GRCh37
NC_000023.9:g.138460852_138461173del NCBI36
NG_007994.1:g.25292_25613del , LRG_556:g.25292_25613del

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.521-35_723+84del
ENST00000643157.1:n.1188-35_1390+84del
ENST00000218099.6:c.521-35_723+84del
ENST00000394090.2:c.407-35_609+84del
NM_000133.3:c.521-35_723+84del , LRG_556t1:c.521-35_723+84del
NM_001313913.1:c.407-35_609+84del
XM_005262397.3:c.392-35_594+84del
XM_005262397.4:c.392-35_594+84del
NM_000133.4:c.521-35_723+84del
NM_001313913.2:c.407-35_609+84del