Canonical Allele Identifier: CA414445354
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 626950
ClinVar RCV Id: RCV000851629
dbSNP Id: rs137852253
MyVariant Identifiers: chrX:g.138643853G>A (hg19) chrX:g.139561694G>A (hg38)
ERepo: CA414445354/MONDO:0010604/080
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561694G>A , CM000685.2:g.139561694G>A GRCh38
NC_000023.10:g.138643853G>A , CM000685.1:g.138643853G>A GRCh37
NC_000023.9:g.138471519G>A NCBI36
NG_007994.1:g.35959G>A , LRG_556:g.35959G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.1009G>A MANE Select ENSP00000218099.2:p.Ala337Thr
ENST00000643157.1:n.1676G>A
ENST00000218099.6:c.1009G>A ENSP00000218099.2:p.Ala337Thr
ENST00000394090.2:c.895G>A ENSP00000377650.2:p.Ala299Thr
NM_000133.3:c.1009G>A , LRG_556t1:c.1009G>A NP_000124.1:p.Ala337Thr
NM_001313913.1:c.895G>A NP_001300842.1:p.Ala299Thr
XM_005262397.3:c.880G>A XP_005262454.1:p.Ala294Thr
XM_005262397.4:c.880G>A XP_005262454.1:p.Ala294Thr
NM_000133.4:c.1009G>A MANE Select NP_000124.1:p.Ala337Thr
NM_001313913.2:c.895G>A NP_001300842.1:p.Ala299Thr
Search 100 bp 5'
Search 100 bp 3'