Canonical Allele Identifier: CA518864002
Gene: F9 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.138644107G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561948G>C , CM000685.2:g.139561948G>C GRCh38
NC_000023.10:g.138644107G>C , CM000685.1:g.138644107G>C GRCh37
NC_000023.9:g.138471773G>C NCBI36
NG_007994.1:g.36213G>C , LRG_556:g.36213G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218099.7:c.1263G>C MANE Select ENSP00000218099.2:p.Gly421=
ENST00000643157.1:n.1723+207G>C
ENST00000218099.6:c.1263G>C ENSP00000218099.2:p.Gly421=
ENST00000394090.2:c.1149G>C ENSP00000377650.2:p.Gly383=
NM_000133.3:c.1263G>C , LRG_556t1:c.1263G>C NP_000124.1:p.Gly421=
NM_001313913.1:c.1149G>C NP_001300842.1:p.Gly383=
XM_005262397.3:c.1134G>C XP_005262454.1:p.Gly378=
XM_005262397.4:c.1134G>C XP_005262454.1:p.Gly378=
NM_000133.4:c.1263G>C MANE Select NP_000124.1:p.Gly421=
NM_001313913.2:c.1149G>C NP_001300842.1:p.Gly383=