Canonical Allele Identifier: CA644672886

Gene: F9

Linked Data

• dbSNP Id: rs1453892590
• gnomAD v2: X-138630397-C-T
• gnomAD v3: X-139548238-C-T
• gnomAD v4: X-139548238-C-T
• MyVariant Identifiers: chrX:g.138630397C>T (hg19) ; chrX:g.139548238C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548238C>T , CM000685.2:g.139548238C>T	GRCh38
NC_000023.10:g.138630397C>T , CM000685.1:g.138630397C>T	GRCh37
NC_000023.9:g.138458063C>T	NCBI36
NG_007994.1:g.22503C>T , LRG_556:g.22503C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-125C>T MANE Select	ENSP00000218099.2:n.392-125C>T
ENST00000643157.1:n.1059-125C>T
ENST00000218099.6:c.392-125C>T	ENSP00000218099.2:n.392-125C>T
ENST00000394090.2:c.278-125C>T	ENSP00000377650.2:n.278-125C>T
ENST00000479617.2:n.345-125C>T
NM_000133.3:c.392-125C>T , LRG_556t1:c.392-125C>T	NP_000124.1:n.392-125C>T
NM_001313913.1:c.278-125C>T	NP_001300842.1:n.278-125C>T
XM_005262397.3:c.392-2824C>T	XP_005262454.1:n.392-2824C>T
XM_005262397.4:c.392-2824C>T	XP_005262454.1:n.392-2824C>T
NM_000133.4:c.392-125C>T MANE Select	NP_000124.1:n.392-125C>T
NM_001313913.2:c.278-125C>T	NP_001300842.1:n.278-125C>T