Canonical Allele Identifier: CA414445653
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561748G>C , CM000685.2:g.139561748G>C GRCh38
NC_000023.10:g.138643907G>C , CM000685.1:g.138643907G>C GRCh37
NC_000023.9:g.138471573G>C NCBI36
NG_007994.1:g.36013G>C , LRG_556:g.36013G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1063G>C MANE Select ENSP00000218099.2:p.Gly355Arg
ENST00000643157.1:n.1723+7G>C
ENST00000218099.6:c.1063G>C ENSP00000218099.2:p.Gly355Arg
ENST00000394090.2:c.949G>C ENSP00000377650.2:p.Gly317Arg
NM_000133.3:c.1063G>C , LRG_556t1:c.1063G>C NP_000124.1:p.Gly355Arg
NM_001313913.1:c.949G>C NP_001300842.1:p.Gly317Arg
XM_005262397.3:c.934G>C XP_005262454.1:p.Gly312Arg
XM_005262397.4:c.934G>C XP_005262454.1:p.Gly312Arg
NM_000133.4:c.1063G>C MANE Select NP_000124.1:p.Gly355Arg
NM_001313913.2:c.949G>C NP_001300842.1:p.Gly317Arg