Canonical Allele Identifier: CA2694839873
Gene: F9 HGNC NCBI

Linked Data

gnomAD v4: X-139561459-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561459T>C , CM000685.2:g.139561459T>C GRCh38
NC_000023.10:g.138643618T>C , CM000685.1:g.138643618T>C GRCh37
NC_000023.9:g.138471284T>C NCBI36
NG_007994.1:g.35724T>C , LRG_556:g.35724T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.839-65T>C MANE Select ENSP00000218099.2:n.839-65T>C
ENST00000643157.1:n.1506-65T>C
ENST00000218099.6:c.839-65T>C ENSP00000218099.2:n.839-65T>C
ENST00000394090.2:c.725-65T>C ENSP00000377650.2:n.725-65T>C
NM_000133.3:c.839-65T>C , LRG_556t1:c.839-65T>C NP_000124.1:n.839-65T>C
NM_001313913.1:c.725-65T>C NP_001300842.1:n.725-65T>C
XM_005262397.3:c.710-65T>C XP_005262454.1:n.710-65T>C
XM_005262397.4:c.710-65T>C XP_005262454.1:n.710-65T>C
NM_000133.4:c.839-65T>C MANE Select NP_000124.1:n.839-65T>C
NM_001313913.2:c.725-65T>C NP_001300842.1:n.725-65T>C
Search 100 bp 5'
Search 100 bp 3'