Canonical Allele Identifier: CA518859421

Gene: F9

Linked Data

• ClinVar Variation Id: 1623620
• ClinVar RCV Id: RCV002110191
• dbSNP Id: rs1556435929
• gnomAD v4: X-139537062-T-C
• MyVariant Identifiers: chrX:g.138619221T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537062T>C , CM000685.2:g.139537062T>C	GRCh38
NC_000023.10:g.138619221T>C , CM000685.1:g.138619221T>C	GRCh37
NC_000023.9:g.138446887T>C	NCBI36
NG_007994.1:g.11327T>C , LRG_556:g.11327T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.141T>C MANE Select	ENSP00000218099.2:p.Tyr47=
ENST00000218099.6:c.141T>C	ENSP00000218099.2:p.Tyr47=
ENST00000394090.2:c.141T>C	ENSP00000377650.2:p.Tyr47=
ENST00000479617.2:n.148T>C
NM_000133.3:c.141T>C , LRG_556t1:c.141T>C	NP_000124.1:p.Tyr47=
NM_001313913.1:c.141T>C	NP_001300842.1:p.Tyr47=
XM_005262397.3:c.141T>C	XP_005262454.1:p.Tyr47=
XM_005262397.4:c.141T>C	XP_005262454.1:p.Tyr47=
NM_000133.4:c.141T>C MANE Select	NP_000124.1:p.Tyr47=
NM_001313913.2:c.141T>C	NP_001300842.1:p.Tyr47=