Canonical Allele Identifier: CA872128664

Gene: F9

Linked Data

• dbSNP Id: rs1207042417
• gnomAD v3: X-139562163-G-A
• gnomAD v4: X-139562163-G-A
• MyVariant Identifiers: chrX:g.138644322G>A (hg19) ; chrX:g.139562163G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562163G>A , CM000685.2:g.139562163G>A	GRCh38
NC_000023.10:g.138644322G>A , CM000685.1:g.138644322G>A	GRCh37
NC_000023.9:g.138471988G>A	NCBI36
NG_007994.1:g.36428G>A , LRG_556:g.36428G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*92G>A MANE Select	ENSP00000218099.2:n.*92G>A
ENST00000643157.1:n.1723+422G>A
ENST00000218099.6:c.*92G>A	ENSP00000218099.2:n.*92G>A
NM_000133.3:c.*92G>A , LRG_556t1:c.*92G>A	NP_000124.1:n.*92G>A
NM_001313913.1:c.*92G>A	NP_001300842.1:n.*92G>A
XM_005262397.3:c.*92G>A	XP_005262454.1:n.*92G>A
XM_005262397.4:c.*92G>A	XP_005262454.1:n.*92G>A
NM_000133.4:c.*92G>A MANE Select	NP_000124.1:n.*92G>A
NM_001313913.2:c.*92G>A	NP_001300842.1:n.*92G>A