Canonical Allele Identifier: CA10529747

Gene: F9

Linked Data

• dbSNP Id: rs756898947
• ExAC: X:138619310 T / G
• gnomAD v4: X-139537151-T-G
• MyVariant Identifiers: chrX:g.138619310T>G (hg19) ; chrX:g.139537151T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139537151T>G , CM000685.2:g.139537151T>G	GRCh38
NC_000023.10:g.138619310T>G , CM000685.1:g.138619310T>G	GRCh37
NC_000023.9:g.138446976T>G	NCBI36
NG_007994.1:g.11416T>G , LRG_556:g.11416T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.230T>G MANE Select	ENSP00000218099.2:p.Val77Gly
ENST00000218099.6:c.230T>G	ENSP00000218099.2:p.Val77Gly
ENST00000394090.2:c.230T>G	ENSP00000377650.2:p.Val77Gly
ENST00000479617.2:n.237T>G
NM_000133.3:c.230T>G , LRG_556t1:c.230T>G	NP_000124.1:p.Val77Gly
NM_001313913.1:c.230T>G	NP_001300842.1:p.Val77Gly
XM_005262397.3:c.230T>G	XP_005262454.1:p.Val77Gly
XM_005262397.4:c.230T>G	XP_005262454.1:p.Val77Gly
NM_000133.4:c.230T>G MANE Select	NP_000124.1:p.Val77Gly
NM_001313913.2:c.230T>G	NP_001300842.1:p.Val77Gly