Canonical Allele Identifier: CA2694839898
Gene: F9 HGNC NCBI

Linked Data

gnomAD v4: X-139562088-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139562088A>C , CM000685.2:g.139562088A>C GRCh38
NC_000023.10:g.138644247A>C , CM000685.1:g.138644247A>C GRCh37
NC_000023.9:g.138471913A>C NCBI36
NG_007994.1:g.36353A>C , LRG_556:g.36353A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.*17A>C MANE Select ENSP00000218099.2:n.*17A>C
ENST00000643157.1:n.1723+347A>C
ENST00000218099.6:c.*17A>C ENSP00000218099.2:n.*17A>C
NM_000133.3:c.*17A>C , LRG_556t1:c.*17A>C NP_000124.1:n.*17A>C
NM_001313913.1:c.*17A>C NP_001300842.1:n.*17A>C
XM_005262397.3:c.*17A>C XP_005262454.1:n.*17A>C
XM_005262397.4:c.*17A>C XP_005262454.1:n.*17A>C
NM_000133.4:c.*17A>C MANE Select NP_000124.1:n.*17A>C
NM_001313913.2:c.*17A>C NP_001300842.1:n.*17A>C
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