Canonical Allele Identifier: CA872128679

Gene: F9

Linked Data

• dbSNP Id: rs1220226764
• gnomAD v3: X-139562189-T-G
• gnomAD v4: X-139562189-T-G
• MyVariant Identifiers: chrX:g.138644348T>G (hg19) ; chrX:g.139562189T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562189T>G , CM000685.2:g.139562189T>G	GRCh38
NC_000023.10:g.138644348T>G , CM000685.1:g.138644348T>G	GRCh37
NC_000023.9:g.138472014T>G	NCBI36
NG_007994.1:g.36454T>G , LRG_556:g.36454T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*118T>G MANE Select	ENSP00000218099.2:n.*118T>G
ENST00000643157.1:n.1723+448T>G
ENST00000218099.6:c.*118T>G	ENSP00000218099.2:n.*118T>G
NM_000133.3:c.*118T>G , LRG_556t1:c.*118T>G	NP_000124.1:n.*118T>G
NM_001313913.1:c.*118T>G	NP_001300842.1:n.*118T>G
XM_005262397.3:c.*118T>G	XP_005262454.1:n.*118T>G
XM_005262397.4:c.*118T>G	XP_005262454.1:n.*118T>G
NM_000133.4:c.*118T>G MANE Select	NP_000124.1:n.*118T>G
NM_001313913.2:c.*118T>G	NP_001300842.1:n.*118T>G