Canonical Allele Identifier: CA2694839175
Gene: F9 HGNC NCBI

Linked Data

gnomAD v4: X-139541020-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139541020G>A , CM000685.2:g.139541020G>A GRCh38
NC_000023.10:g.138623179G>A , CM000685.1:g.138623179G>A GRCh37
NC_000023.9:g.138450845G>A NCBI36
NG_007994.1:g.15285G>A , LRG_556:g.15285G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.278-56G>A MANE Select ENSP00000218099.2:n.278-56G>A
ENST00000218099.6:c.278-56G>A ENSP00000218099.2:n.278-56G>A
ENST00000394090.2:c.277+3634G>A ENSP00000377650.2:n.277+3634G>A
ENST00000479617.2:n.242-67G>A
NM_000133.3:c.278-56G>A , LRG_556t1:c.278-56G>A NP_000124.1:n.278-56G>A
NM_001313913.1:c.277+3634G>A NP_001300842.1:n.277+3634G>A
XM_005262397.3:c.278-56G>A XP_005262454.1:n.278-56G>A
XM_005262397.4:c.278-56G>A XP_005262454.1:n.278-56G>A
NM_000133.4:c.278-56G>A MANE Select NP_000124.1:n.278-56G>A
NM_001313913.2:c.277+3634G>A NP_001300842.1:n.277+3634G>A
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