Canonical Allele Identifier: CA414444985

Gene: F9

Linked Data

• dbSNP Id: rs1222617621
• gnomAD v2: X-138643808-G-A
• gnomAD v3: X-139561649-G-A
• gnomAD v4: X-139561649-G-A
• MyVariant Identifiers: chrX:g.138643808G>A (hg19) ; chrX:g.139561649G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561649G>A , CM000685.2:g.139561649G>A	GRCh38
NC_000023.10:g.138643808G>A , CM000685.1:g.138643808G>A	GRCh37
NC_000023.9:g.138471474G>A	NCBI36
NG_007994.1:g.35914G>A , LRG_556:g.35914G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.964G>A MANE Select	ENSP00000218099.2:p.Asp322Asn
ENST00000643157.1:n.1631G>A
ENST00000218099.6:c.964G>A	ENSP00000218099.2:p.Asp322Asn
ENST00000394090.2:c.850G>A	ENSP00000377650.2:p.Asp284Asn
NM_000133.3:c.964G>A , LRG_556t1:c.964G>A	NP_000124.1:p.Asp322Asn
NM_001313913.1:c.850G>A	NP_001300842.1:p.Asp284Asn
XM_005262397.3:c.835G>A	XP_005262454.1:p.Asp279Asn
XM_005262397.4:c.835G>A	XP_005262454.1:p.Asp279Asn
NM_000133.4:c.964G>A MANE Select	NP_000124.1:p.Asp322Asn
NM_001313913.2:c.850G>A	NP_001300842.1:p.Asp284Asn