Canonical Allele Identifier: CA414438753

Gene: F9

Linked Data

• ClinVar Variation Id: 811514
• ClinVar RCV Id: RCV001001429
• dbSNP Id: rs1603265480
• MyVariant Identifiers: chrX:g.138630521G>C (hg19) ; chrX:g.139548362G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548362G>C , CM000685.2:g.139548362G>C	GRCh38
NC_000023.10:g.138630521G>C , CM000685.1:g.138630521G>C	GRCh37
NC_000023.9:g.138458187G>C	NCBI36
NG_007994.1:g.22627G>C , LRG_556:g.22627G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-1G>C MANE Select	ENSP00000218099.2:n.392-1G>C
ENST00000643157.1:n.1059-1G>C
ENST00000218099.6:c.392-1G>C	ENSP00000218099.2:n.392-1G>C
ENST00000394090.2:c.278-1G>C	ENSP00000377650.2:n.278-1G>C
ENST00000479617.2:n.345-1G>C
NM_000133.3:c.392-1G>C , LRG_556t1:c.392-1G>C	NP_000124.1:n.392-1G>C
NM_001313913.1:c.278-1G>C	NP_001300842.1:n.278-1G>C
XM_005262397.3:c.392-2700G>C	XP_005262454.1:n.392-2700G>C
XM_005262397.4:c.392-2700G>C	XP_005262454.1:n.392-2700G>C
NM_000133.4:c.392-1G>C MANE Select	NP_000124.1:n.392-1G>C
NM_001313913.2:c.278-1G>C	NP_001300842.1:n.278-1G>C