Canonical Allele Identifier: CA644670733

Gene: F9

Linked Data

• dbSNP Id: rs1251816730
• gnomAD v2: X-138623190-C-A
• gnomAD v3: X-139541031-C-A
• gnomAD v4: X-139541031-C-A
• MyVariant Identifiers: chrX:g.138623190C>A (hg19) ; chrX:g.139541031C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541031C>A , CM000685.2:g.139541031C>A	GRCh38
NC_000023.10:g.138623190C>A , CM000685.1:g.138623190C>A	GRCh37
NC_000023.9:g.138450856C>A	NCBI36
NG_007994.1:g.15296C>A , LRG_556:g.15296C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.278-45C>A MANE Select	ENSP00000218099.2:n.278-45C>A
ENST00000218099.6:c.278-45C>A	ENSP00000218099.2:n.278-45C>A
ENST00000394090.2:c.277+3645C>A	ENSP00000377650.2:n.277+3645C>A
ENST00000479617.2:n.242-56C>A
NM_000133.3:c.278-45C>A , LRG_556t1:c.278-45C>A	NP_000124.1:n.278-45C>A
NM_001313913.1:c.277+3645C>A	NP_001300842.1:n.277+3645C>A
XM_005262397.3:c.278-45C>A	XP_005262454.1:n.278-45C>A
XM_005262397.4:c.278-45C>A	XP_005262454.1:n.278-45C>A
NM_000133.4:c.278-45C>A MANE Select	NP_000124.1:n.278-45C>A
NM_001313913.2:c.277+3645C>A	NP_001300842.1:n.277+3645C>A