Canonical Allele Identifier: CA255324
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 10577
ClinVar RCV Id: RCV000011323
dbSNP Id: rs137852231
MyVariant Identifiers: chrX:g.138623244A>C (hg19) chrX:g.139541085A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139541085A>C , CM000685.2:g.139541085A>C GRCh38
NC_000023.10:g.138623244A>C , CM000685.1:g.138623244A>C GRCh37
NC_000023.9:g.138450910A>C NCBI36
NG_007994.1:g.15350A>C , LRG_556:g.15350A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.287A>C MANE Select ENSP00000218099.2:p.Gln96Pro
ENST00000218099.6:c.287A>C ENSP00000218099.2:p.Gln96Pro
ENST00000394090.2:c.277+3699A>C ENSP00000377650.2:n.277+3699A>C
ENST00000479617.2:n.242-2A>C
NM_000133.3:c.287A>C , LRG_556t1:c.287A>C NP_000124.1:p.Gln96Pro
NM_001313913.1:c.277+3699A>C NP_001300842.1:n.277+3699A>C
XM_005262397.3:c.287A>C XP_005262454.1:p.Gln96Pro
XM_005262397.4:c.287A>C XP_005262454.1:p.Gln96Pro
NM_000133.4:c.287A>C MANE Select NP_000124.1:p.Gln96Pro
NM_001313913.2:c.277+3699A>C NP_001300842.1:n.277+3699A>C
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