Canonical Allele Identifier: CA644676933

Gene: F9

Linked Data

• dbSNP Id: rs1191212755
• gnomAD v2: X-138643028-A-G
• gnomAD v4: X-139560869-A-G
• MyVariant Identifiers: chrX:g.138643028A>G (hg19) ; chrX:g.139560869A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560869A>G , CM000685.2:g.139560869A>G	GRCh38
NC_000023.10:g.138643028A>G , CM000685.1:g.138643028A>G	GRCh37
NC_000023.9:g.138470694A>G	NCBI36
NG_007994.1:g.35134A>G , LRG_556:g.35134A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.838+14A>G MANE Select	ENSP00000218099.2:n.838+14A>G
ENST00000643157.1:n.1505+14A>G
ENST00000218099.6:c.838+14A>G	ENSP00000218099.2:n.838+14A>G
ENST00000394090.2:c.724+14A>G	ENSP00000377650.2:n.724+14A>G
NM_000133.3:c.838+14A>G , LRG_556t1:c.838+14A>G	NP_000124.1:n.838+14A>G
NM_001313913.1:c.724+14A>G	NP_001300842.1:n.724+14A>G
XM_005262397.3:c.709+14A>G	XP_005262454.1:n.709+14A>G
XM_005262397.4:c.709+14A>G	XP_005262454.1:n.709+14A>G
NM_000133.4:c.838+14A>G MANE Select	NP_000124.1:n.838+14A>G
NM_001313913.2:c.724+14A>G	NP_001300842.1:n.724+14A>G