Canonical Allele Identifier: CA872127435

Gene: F9

Linked Data

• dbSNP Id: rs1184916853
• MyVariant Identifiers: chrX:g.138643640T>C (hg19) ; chrX:g.139561481T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561481T>C , CM000685.2:g.139561481T>C	GRCh38
NC_000023.10:g.138643640T>C , CM000685.1:g.138643640T>C	GRCh37
NC_000023.9:g.138471306T>C	NCBI36
NG_007994.1:g.35746T>C , LRG_556:g.35746T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.839-43T>C MANE Select	ENSP00000218099.2:n.839-43T>C
ENST00000643157.1:n.1506-43T>C
ENST00000218099.6:c.839-43T>C	ENSP00000218099.2:n.839-43T>C
ENST00000394090.2:c.725-43T>C	ENSP00000377650.2:n.725-43T>C
NM_000133.3:c.839-43T>C , LRG_556t1:c.839-43T>C	NP_000124.1:n.839-43T>C
NM_001313913.1:c.725-43T>C	NP_001300842.1:n.725-43T>C
XM_005262397.3:c.710-43T>C	XP_005262454.1:n.710-43T>C
XM_005262397.4:c.710-43T>C	XP_005262454.1:n.710-43T>C
NM_000133.4:c.839-43T>C MANE Select	NP_000124.1:n.839-43T>C
NM_001313913.2:c.725-43T>C	NP_001300842.1:n.725-43T>C