Canonical Allele Identifier: CA10529895
Gene: F9 HGNC NCBI

Linked Data

ClinVar Variation Id: 990714
ClinVar RCV Id: RCV001278796
dbSNP Id: rs186616567
ExAC: X:138644240 G / C
gnomAD v2: X-138644240-G-C
gnomAD v3: X-139562081-G-C
gnomAD v4: X-139562081-G-C
MyVariant Identifiers: chrX:g.138644240G>C (hg19) chrX:g.139562081G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562081G>C , CM000685.2:g.139562081G>C GRCh38
NC_000023.10:g.138644240G>C , CM000685.1:g.138644240G>C GRCh37
NC_000023.9:g.138471906G>C NCBI36
NG_007994.1:g.36346G>C , LRG_556:g.36346G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.*10G>C MANE Select ENSP00000218099.2:n.*10G>C
ENST00000643157.1:n.1723+340G>C
ENST00000218099.6:c.*10G>C ENSP00000218099.2:n.*10G>C
NM_000133.3:c.*10G>C , LRG_556t1:c.*10G>C NP_000124.1:n.*10G>C
NM_001313913.1:c.*10G>C NP_001300842.1:n.*10G>C
XM_005262397.3:c.*10G>C XP_005262454.1:n.*10G>C
XM_005262397.4:c.*10G>C XP_005262454.1:n.*10G>C
NM_000133.4:c.*10G>C MANE Select NP_000124.1:n.*10G>C
NM_001313913.2:c.*10G>C NP_001300842.1:n.*10G>C
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