Canonical Allele Identifier: CA644677229

Gene: F9

Linked Data

• dbSNP Id: rs1387488120
• gnomAD v2: X-138644250-G-T
• gnomAD v4: X-139562091-G-T
• MyVariant Identifiers: chrX:g.138644250G>T (hg19) ; chrX:g.139562091G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562091G>T , CM000685.2:g.139562091G>T	GRCh38
NC_000023.10:g.138644250G>T , CM000685.1:g.138644250G>T	GRCh37
NC_000023.9:g.138471916G>T	NCBI36
NG_007994.1:g.36356G>T , LRG_556:g.36356G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*20G>T MANE Select	ENSP00000218099.2:n.*20G>T
ENST00000643157.1:n.1723+350G>T
ENST00000218099.6:c.*20G>T	ENSP00000218099.2:n.*20G>T
NM_000133.3:c.*20G>T , LRG_556t1:c.*20G>T	NP_000124.1:n.*20G>T
NM_001313913.1:c.*20G>T	NP_001300842.1:n.*20G>T
XM_005262397.3:c.*20G>T	XP_005262454.1:n.*20G>T
XM_005262397.4:c.*20G>T	XP_005262454.1:n.*20G>T
NM_000133.4:c.*20G>T MANE Select	NP_000124.1:n.*20G>T
NM_001313913.2:c.*20G>T	NP_001300842.1:n.*20G>T