Canonical Allele Identifier: CA644677222

Gene: F9

Linked Data

• dbSNP Id: rs1402233903
• gnomAD v2: X-138644233-A-G
• gnomAD v3: X-139562074-A-G
• gnomAD v4: X-139562074-A-G
• MyVariant Identifiers: chrX:g.138644233A>G (hg19) ; chrX:g.139562074A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562074A>G , CM000685.2:g.139562074A>G	GRCh38
NC_000023.10:g.138644233A>G , CM000685.1:g.138644233A>G	GRCh37
NC_000023.9:g.138471899A>G	NCBI36
NG_007994.1:g.36339A>G , LRG_556:g.36339A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*3A>G MANE Select	ENSP00000218099.2:n.*3A>G
ENST00000643157.1:n.1723+333A>G
ENST00000218099.6:c.*3A>G	ENSP00000218099.2:n.*3A>G
NM_000133.3:c.*3A>G , LRG_556t1:c.*3A>G	NP_000124.1:n.*3A>G
NM_001313913.1:c.*3A>G	NP_001300842.1:n.*3A>G
XM_005262397.3:c.*3A>G	XP_005262454.1:n.*3A>G
XM_005262397.4:c.*3A>G	XP_005262454.1:n.*3A>G
NM_000133.4:c.*3A>G MANE Select	NP_000124.1:n.*3A>G
NM_001313913.2:c.*3A>G	NP_001300842.1:n.*3A>G