Canonical Allele Identifier: CA336143583
Gene: F9 HGNC NCBI

Linked Data

dbSNP Id: rs748081916
gnomAD v3: X-139562201-CA-C
gnomAD v4: X-139562201-CA-C
MyVariant Identifiers: chrX:g.138644361del (hg19) chrX:g.139562202del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562202del , CM000685.2:g.139562202del GRCh38
NC_000023.10:g.138644361del , CM000685.1:g.138644361del GRCh37
NC_000023.9:g.138472027del NCBI36
NG_007994.1:g.36467del , LRG_556:g.36467del

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.*131del MANE Select ENSP00000218099.2:n.*131del
ENST00000643157.1:n.1723+461del
ENST00000218099.6:c.*131del ENSP00000218099.2:n.*131del
NM_000133.3:c.*131del , LRG_556t1:c.*131del NP_000124.1:n.*131del
NM_001313913.1:c.*131del NP_001300842.1:n.*131del
XM_005262397.3:c.*131del XP_005262454.1:n.*131del
XM_005262397.4:c.*131del XP_005262454.1:n.*131del
NM_000133.4:c.*131del MANE Select NP_000124.1:n.*131del
NM_001313913.2:c.*131del NP_001300842.1:n.*131del
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