Canonical Allele Identifier: CA518862953

Gene: F9

Linked Data

• ClinVar Variation Id: 1648981
• ClinVar RCV Id: RCV002144112
• dbSNP Id: rs2148367218
• MyVariant Identifiers: chrX:g.138642923T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560764T>C , CM000685.2:g.139560764T>C	GRCh38
NC_000023.10:g.138642923T>C , CM000685.1:g.138642923T>C	GRCh37
NC_000023.9:g.138470589T>C	NCBI36
NG_007994.1:g.35029T>C , LRG_556:g.35029T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.747T>C MANE Select	ENSP00000218099.2:p.Asp249=
ENST00000643157.1:n.1414T>C
ENST00000218099.6:c.747T>C	ENSP00000218099.2:p.Asp249=
ENST00000394090.2:c.633T>C	ENSP00000377650.2:p.Asp211=
NM_000133.3:c.747T>C , LRG_556t1:c.747T>C	NP_000124.1:p.Asp249=
NM_001313913.1:c.633T>C	NP_001300842.1:p.Asp211=
XM_005262397.3:c.618T>C	XP_005262454.1:p.Asp206=
XM_005262397.4:c.618T>C	XP_005262454.1:p.Asp206=
NM_000133.4:c.747T>C MANE Select	NP_000124.1:p.Asp249=
NM_001313913.2:c.633T>C	NP_001300842.1:p.Asp211=