Canonical Allele Identifier: CA518859357
Gene: F9 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.138619209G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139537050G>C , CM000685.2:g.139537050G>C GRCh38
NC_000023.10:g.138619209G>C , CM000685.1:g.138619209G>C GRCh37
NC_000023.9:g.138446875G>C NCBI36
NG_007994.1:g.11315G>C , LRG_556:g.11315G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.129G>C MANE Select ENSP00000218099.2:p.Arg43=
ENST00000218099.6:c.129G>C ENSP00000218099.2:p.Arg43=
ENST00000394090.2:c.129G>C ENSP00000377650.2:p.Arg43=
ENST00000479617.2:n.136G>C
NM_000133.3:c.129G>C , LRG_556t1:c.129G>C NP_000124.1:p.Arg43=
NM_001313913.1:c.129G>C NP_001300842.1:p.Arg43=
XM_005262397.3:c.129G>C XP_005262454.1:p.Arg43=
XM_005262397.4:c.129G>C XP_005262454.1:p.Arg43=
NM_000133.4:c.129G>C MANE Select NP_000124.1:p.Arg43=
NM_001313913.2:c.129G>C NP_001300842.1:p.Arg43=
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