Canonical Allele Identifier: CA872122143

Gene: F9

Linked Data

• dbSNP Id: rs1240997435
• gnomAD v3: X-139550940-A-T
• gnomAD v4: X-139550940-A-T
• MyVariant Identifiers: chrX:g.138633099A>T (hg19) ; chrX:g.139550940A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139550940A>T , CM000685.2:g.139550940A>T	GRCh38
NC_000023.10:g.138633099A>T , CM000685.1:g.138633099A>T	GRCh37
NC_000023.9:g.138460765A>T	NCBI36
NG_007994.1:g.25205A>T , LRG_556:g.25205A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.521-122A>T MANE Select	ENSP00000218099.2:n.521-122A>T
ENST00000643157.1:n.1188-122A>T
ENST00000218099.6:c.521-122A>T	ENSP00000218099.2:n.521-122A>T
ENST00000394090.2:c.407-122A>T	ENSP00000377650.2:n.407-122A>T
NM_000133.3:c.521-122A>T , LRG_556t1:c.521-122A>T	NP_000124.1:n.521-122A>T
NM_001313913.1:c.407-122A>T	NP_001300842.1:n.407-122A>T
XM_005262397.3:c.392-122A>T	XP_005262454.1:n.392-122A>T
XM_005262397.4:c.392-122A>T	XP_005262454.1:n.392-122A>T
NM_000133.4:c.521-122A>T MANE Select	NP_000124.1:n.521-122A>T
NM_001313913.2:c.407-122A>T	NP_001300842.1:n.407-122A>T