Canonical Allele Identifier: CA644672926

Gene: F9

Linked Data

• dbSNP Id: rs752747648
• gnomAD v2: X-138630506-A-C
• gnomAD v4: X-139548347-A-C
• MyVariant Identifiers: chrX:g.138630506A>C (hg19) ; chrX:g.139548347A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548347A>C , CM000685.2:g.139548347A>C	GRCh38
NC_000023.10:g.138630506A>C , CM000685.1:g.138630506A>C	GRCh37
NC_000023.9:g.138458172A>C	NCBI36
NG_007994.1:g.22612A>C , LRG_556:g.22612A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-16A>C MANE Select	ENSP00000218099.2:n.392-16A>C
ENST00000643157.1:n.1059-16A>C
ENST00000218099.6:c.392-16A>C	ENSP00000218099.2:n.392-16A>C
ENST00000394090.2:c.278-16A>C	ENSP00000377650.2:n.278-16A>C
ENST00000479617.2:n.345-16A>C
NM_000133.3:c.392-16A>C , LRG_556t1:c.392-16A>C	NP_000124.1:n.392-16A>C
NM_001313913.1:c.278-16A>C	NP_001300842.1:n.278-16A>C
XM_005262397.3:c.392-2715A>C	XP_005262454.1:n.392-2715A>C
XM_005262397.4:c.392-2715A>C	XP_005262454.1:n.392-2715A>C
NM_000133.4:c.392-16A>C MANE Select	NP_000124.1:n.392-16A>C
NM_001313913.2:c.278-16A>C	NP_001300842.1:n.278-16A>C