Canonical Allele Identifier: CA2694839863
Gene: F9 HGNC NCBI

Linked Data

gnomAD v4: X-139561442-T-TC
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561443dup , CM000685.2:g.139561443dup GRCh38
NC_000023.10:g.138643602dup , CM000685.1:g.138643602dup GRCh37
NC_000023.9:g.138471268dup NCBI36
NG_007994.1:g.35708dup , LRG_556:g.35708dup

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.839-81dup MANE Select ENSP00000218099.2:n.839-81dup
ENST00000643157.1:n.1506-81dup
ENST00000218099.6:c.839-81dup ENSP00000218099.2:n.839-81dup
ENST00000394090.2:c.725-81dup ENSP00000377650.2:n.725-81dup
NM_000133.3:c.839-81dup , LRG_556t1:c.839-81dup NP_000124.1:n.839-81dup
NM_001313913.1:c.725-81dup NP_001300842.1:n.725-81dup
XM_005262397.3:c.710-81dup XP_005262454.1:n.710-81dup
XM_005262397.4:c.710-81dup XP_005262454.1:n.710-81dup
NM_000133.4:c.839-81dup MANE Select NP_000124.1:n.839-81dup
NM_001313913.2:c.725-81dup NP_001300842.1:n.725-81dup
Search 100 bp 5'
Search 100 bp 3'