Canonical Allele Identifier: CA10529813
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2927807
ClinVar RCV Id: RCV003784437
dbSNP Id: rs755283462
ExAC: X:138633303 T / C
gnomAD v2: X-138633303-T-C
COSMIC: COSM4638073
MyVariant Identifiers: chrX:g.138633303T>C (hg19) chrX:g.139551144T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139551144T>C , CM000685.2:g.139551144T>C GRCh38
NC_000023.10:g.138633303T>C , CM000685.1:g.138633303T>C GRCh37
NC_000023.9:g.138460969T>C NCBI36
NG_007994.1:g.25409T>C , LRG_556:g.25409T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.603T>C MANE Select ENSP00000218099.2:p.Tyr201=
ENST00000643157.1:n.1270T>C
ENST00000218099.6:c.603T>C ENSP00000218099.2:p.Tyr201=
ENST00000394090.2:c.489T>C ENSP00000377650.2:p.Tyr163=
NM_000133.3:c.603T>C , LRG_556t1:c.603T>C NP_000124.1:p.Tyr201=
NM_001313913.1:c.489T>C NP_001300842.1:p.Tyr163=
XM_005262397.3:c.474T>C XP_005262454.1:p.Tyr158=
XM_005262397.4:c.474T>C XP_005262454.1:p.Tyr158=
NM_000133.4:c.603T>C MANE Select NP_000124.1:p.Tyr201=
NM_001313913.2:c.489T>C NP_001300842.1:p.Tyr163=
Search 100 bp 5'
Search 100 bp 3'