Canonical Allele Identifier: CA2694839771
Gene: F9 HGNC NCBI

Linked Data

gnomAD v4: X-139560729-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139560729T>C , CM000685.2:g.139560729T>C GRCh38
NC_000023.10:g.138642888T>C , CM000685.1:g.138642888T>C GRCh37
NC_000023.9:g.138470554T>C NCBI36
NG_007994.1:g.34994T>C , LRG_556:g.34994T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.724-12T>C MANE Select ENSP00000218099.2:n.724-12T>C
ENST00000643157.1:n.1391-12T>C
ENST00000218099.6:c.724-12T>C ENSP00000218099.2:n.724-12T>C
ENST00000394090.2:c.610-12T>C ENSP00000377650.2:n.610-12T>C
NM_000133.3:c.724-12T>C , LRG_556t1:c.724-12T>C NP_000124.1:n.724-12T>C
NM_001313913.1:c.610-12T>C NP_001300842.1:n.610-12T>C
XM_005262397.3:c.595-12T>C XP_005262454.1:n.595-12T>C
XM_005262397.4:c.595-12T>C XP_005262454.1:n.595-12T>C
NM_000133.4:c.724-12T>C MANE Select NP_000124.1:n.724-12T>C
NM_001313913.2:c.610-12T>C NP_001300842.1:n.610-12T>C
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