Canonical Allele Identifier: CA518916426
Gene: F9 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.138643741T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561582T>A , CM000685.2:g.139561582T>A GRCh38
NC_000023.10:g.138643741T>A , CM000685.1:g.138643741T>A GRCh37
NC_000023.9:g.138471407T>A NCBI36
NG_007994.1:g.35847T>A , LRG_556:g.35847T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.897T>A MANE Select ENSP00000218099.2:p.Ile299=
ENST00000643157.1:n.1564T>A
ENST00000218099.6:c.897T>A ENSP00000218099.2:p.Ile299=
ENST00000394090.2:c.783T>A ENSP00000377650.2:p.Ile261=
NM_000133.3:c.897T>A , LRG_556t1:c.897T>A NP_000124.1:p.Ile299=
NM_001313913.1:c.783T>A NP_001300842.1:p.Ile261=
XM_005262397.3:c.768T>A XP_005262454.1:p.Ile256=
XM_005262397.4:c.768T>A XP_005262454.1:p.Ile256=
NM_000133.4:c.897T>A MANE Select NP_000124.1:p.Ile299=
NM_001313913.2:c.783T>A NP_001300842.1:p.Ile261=