Canonical Allele Identifier: CA336128584
Community Standard Title: NM_000133.4(F9):c.88+75A>G
Gene: F9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139530927A>G , CM000685.2:g.139530927A>G GRCh38
NC_000023.10:g.138613086A>G , CM000685.1:g.138613086A>G GRCh37
NC_000023.9:g.138440752A>G NCBI36
NG_007994.1:g.5192A>G , LRG_556:g.5192A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000133.4:c.88+75A>G MANE Select NP_000124.1:n.88+75A>G
ENST00000218099.7:c.88+75A>G MANE Select ENSP00000218099.2:n.88+75A>G
NM_000133.3:c.88+75A>G , LRG_556t1:c.88+75A>G NP_000124.1:n.88+75A>G
NM_001313913.1:c.88+75A>G NP_001300842.1:n.88+75A>G
NM_001313913.2:c.88+75A>G NP_001300842.1:n.88+75A>G
ENST00000218099.6:c.88+75A>G ENSP00000218099.2:n.88+75A>G
ENST00000394090.2:c.88+75A>G ENSP00000377650.2:n.88+75A>G
ENST00000479617.2:n.95+75A>G
XM_005262397.3:c.88+75A>G XP_005262454.1:n.88+75A>G
XM_005262397.4:c.88+75A>G XP_005262454.1:n.88+75A>G
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