Canonical Allele Identifier: CA414438767

Gene: F9

Linked Data

• dbSNP Id: rs1927764460
• MyVariant Identifiers: chrX:g.138630524G>A (hg19) ; chrX:g.139548365G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548365G>A , CM000685.2:g.139548365G>A	GRCh38
NC_000023.10:g.138630524G>A , CM000685.1:g.138630524G>A	GRCh37
NC_000023.9:g.138458190G>A	NCBI36
NG_007994.1:g.22630G>A , LRG_556:g.22630G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.394G>A MANE Select	ENSP00000218099.2:p.Val132Ile
ENST00000643157.1:n.1061G>A
ENST00000218099.6:c.394G>A	ENSP00000218099.2:p.Val132Ile
ENST00000394090.2:c.280G>A	ENSP00000377650.2:p.Val94Ile
ENST00000479617.2:n.347G>A
NM_000133.3:c.394G>A , LRG_556t1:c.394G>A	NP_000124.1:p.Val132Ile
NM_001313913.1:c.280G>A	NP_001300842.1:p.Val94Ile
XM_005262397.3:c.392-2697G>A	XP_005262454.1:n.392-2697G>A
XM_005262397.4:c.392-2697G>A	XP_005262454.1:n.392-2697G>A
NM_000133.4:c.394G>A MANE Select	NP_000124.1:p.Val132Ile
NM_001313913.2:c.280G>A	NP_001300842.1:p.Val94Ile