Canonical Allele Identifier: CA414444894
Gene: F9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561631A>C , CM000685.2:g.139561631A>C GRCh38
NC_000023.10:g.138643790A>C , CM000685.1:g.138643790A>C GRCh37
NC_000023.9:g.138471456A>C NCBI36
NG_007994.1:g.35896A>C , LRG_556:g.35896A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.946A>C MANE Select ENSP00000218099.2:p.Ile316Leu
ENST00000643157.1:n.1613A>C
ENST00000218099.6:c.946A>C ENSP00000218099.2:p.Ile316Leu
ENST00000394090.2:c.832A>C ENSP00000377650.2:p.Ile278Leu
NM_000133.3:c.946A>C , LRG_556t1:c.946A>C NP_000124.1:p.Ile316Leu
NM_001313913.1:c.832A>C NP_001300842.1:p.Ile278Leu
XM_005262397.3:c.817A>C XP_005262454.1:p.Ile273Leu
XM_005262397.4:c.817A>C XP_005262454.1:p.Ile273Leu
NM_000133.4:c.946A>C MANE Select NP_000124.1:p.Ile316Leu
NM_001313913.2:c.832A>C NP_001300842.1:p.Ile278Leu
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