Canonical Allele Identifier: CA518861681

Gene: F9

Linked Data

• gnomAD v4: X-139551129-T-C
• MyVariant Identifiers: chrX:g.138633288T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551129T>C , CM000685.2:g.139551129T>C	GRCh38
NC_000023.10:g.138633288T>C , CM000685.1:g.138633288T>C	GRCh37
NC_000023.9:g.138460954T>C	NCBI36
NG_007994.1:g.25394T>C , LRG_556:g.25394T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.588T>C MANE Select	ENSP00000218099.2:p.Phe196=
ENST00000643157.1:n.1255T>C
ENST00000218099.6:c.588T>C	ENSP00000218099.2:p.Phe196=
ENST00000394090.2:c.474T>C	ENSP00000377650.2:p.Phe158=
NM_000133.3:c.588T>C , LRG_556t1:c.588T>C	NP_000124.1:p.Phe196=
NM_001313913.1:c.474T>C	NP_001300842.1:p.Phe158=
XM_005262397.3:c.459T>C	XP_005262454.1:p.Phe153=
XM_005262397.4:c.459T>C	XP_005262454.1:p.Phe153=
NM_000133.4:c.588T>C MANE Select	NP_000124.1:p.Phe196=
NM_001313913.2:c.474T>C	NP_001300842.1:p.Phe158=