Canonical Allele Identifier: CA414440688
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139551139G>C , CM000685.2:g.139551139G>C GRCh38
NC_000023.10:g.138633298G>C , CM000685.1:g.138633298G>C GRCh37
NC_000023.9:g.138460964G>C NCBI36
NG_007994.1:g.25404G>C , LRG_556:g.25404G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.598G>C MANE Select ENSP00000218099.2:p.Asp200His
ENST00000643157.1:n.1265G>C
ENST00000218099.6:c.598G>C ENSP00000218099.2:p.Asp200His
ENST00000394090.2:c.484G>C ENSP00000377650.2:p.Asp162His
NM_000133.3:c.598G>C , LRG_556t1:c.598G>C NP_000124.1:p.Asp200His
NM_001313913.1:c.484G>C NP_001300842.1:p.Asp162His
XM_005262397.3:c.469G>C XP_005262454.1:p.Asp157His
XM_005262397.4:c.469G>C XP_005262454.1:p.Asp157His
NM_000133.4:c.598G>C MANE Select NP_000124.1:p.Asp200His
NM_001313913.2:c.484G>C NP_001300842.1:p.Asp162His