Canonical Allele Identifier: CA414441093

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138633369C>G (hg19) ; chrX:g.139551210C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551210C>G , CM000685.2:g.139551210C>G	GRCh38
NC_000023.10:g.138633369C>G , CM000685.1:g.138633369C>G	GRCh37
NC_000023.9:g.138461035C>G	NCBI36
NG_007994.1:g.25475C>G , LRG_556:g.25475C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.669C>G MANE Select	ENSP00000218099.2:p.Asp223Glu
ENST00000643157.1:n.1336C>G
ENST00000218099.6:c.669C>G	ENSP00000218099.2:p.Asp223Glu
ENST00000394090.2:c.555C>G	ENSP00000377650.2:p.Asp185Glu
NM_000133.3:c.669C>G , LRG_556t1:c.669C>G	NP_000124.1:p.Asp223Glu
NM_001313913.1:c.555C>G	NP_001300842.1:p.Asp185Glu
XM_005262397.3:c.540C>G	XP_005262454.1:p.Asp180Glu
XM_005262397.4:c.540C>G	XP_005262454.1:p.Asp180Glu
NM_000133.4:c.669C>G MANE Select	NP_000124.1:p.Asp223Glu
NM_001313913.2:c.555C>G	NP_001300842.1:p.Asp185Glu