Canonical Allele Identifier: CA414436498

Gene: F9

Linked Data

• ClinVar Variation Id: 574429
• ClinVar RCV Id: RCV000696357
• dbSNP Id: rs1434866164
• MyVariant Identifiers: chrX:g.138619520G>C (hg19) ; chrX:g.139537361G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537361G>C , CM000685.2:g.139537361G>C	GRCh38
NC_000023.10:g.138619520G>C , CM000685.1:g.138619520G>C	GRCh37
NC_000023.9:g.138447186G>C	NCBI36
NG_007994.1:g.11626G>C , LRG_556:g.11626G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.253-1G>C MANE Select	ENSP00000218099.2:n.253-1G>C
ENST00000218099.6:c.253-1G>C	ENSP00000218099.2:n.253-1G>C
ENST00000394090.2:c.253-1G>C	ENSP00000377650.2:n.253-1G>C
ENST00000479617.2:n.241+206G>C
NM_000133.3:c.253-1G>C , LRG_556t1:c.253-1G>C	NP_000124.1:n.253-1G>C
NM_001313913.1:c.253-1G>C	NP_001300842.1:n.253-1G>C
XM_005262397.3:c.253-1G>C	XP_005262454.1:n.253-1G>C
XM_005262397.4:c.253-1G>C	XP_005262454.1:n.253-1G>C
NM_000133.4:c.253-1G>C MANE Select	NP_000124.1:n.253-1G>C
NM_001313913.2:c.253-1G>C	NP_001300842.1:n.253-1G>C