Canonical Allele Identifier: CA10529773
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2169796
ClinVar RCV Id: RCV003093254
dbSNP Id: rs751604122
ExAC: X:138623251 G / A
gnomAD v2: X-138623251-G-A
gnomAD v4: X-139541092-G-A
MyVariant Identifiers: chrX:g.138623251G>A (hg19) chrX:g.139541092G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139541092G>A , CM000685.2:g.139541092G>A GRCh38
NC_000023.10:g.138623251G>A , CM000685.1:g.138623251G>A GRCh37
NC_000023.9:g.138450917G>A NCBI36
NG_007994.1:g.15357G>A , LRG_556:g.15357G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.294G>A MANE Select ENSP00000218099.2:p.Glu98=
ENST00000218099.6:c.294G>A ENSP00000218099.2:p.Glu98=
ENST00000394090.2:c.277+3706G>A ENSP00000377650.2:n.277+3706G>A
ENST00000479617.2:n.247G>A
NM_000133.3:c.294G>A , LRG_556t1:c.294G>A NP_000124.1:p.Glu98=
NM_001313913.1:c.277+3706G>A NP_001300842.1:n.277+3706G>A
XM_005262397.3:c.294G>A XP_005262454.1:p.Glu98=
XM_005262397.4:c.294G>A XP_005262454.1:p.Glu98=
NM_000133.4:c.294G>A MANE Select NP_000124.1:p.Glu98=
NM_001313913.2:c.277+3706G>A NP_001300842.1:n.277+3706G>A
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