Canonical Allele Identifier: CA414441172

Gene: F9

Linked Data

• COSMIC: COSM3363836
• MyVariant Identifiers: chrX:g.138633386G>T (hg19) ; chrX:g.139551227G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551227G>T , CM000685.2:g.139551227G>T	GRCh38
NC_000023.10:g.138633386G>T , CM000685.1:g.138633386G>T	GRCh37
NC_000023.9:g.138461052G>T	NCBI36
NG_007994.1:g.25492G>T , LRG_556:g.25492G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.686G>T MANE Select	ENSP00000218099.2:p.Gly229Val
ENST00000643157.1:n.1353G>T
ENST00000218099.6:c.686G>T	ENSP00000218099.2:p.Gly229Val
ENST00000394090.2:c.572G>T	ENSP00000377650.2:p.Gly191Val
NM_000133.3:c.686G>T , LRG_556t1:c.686G>T	NP_000124.1:p.Gly229Val
NM_001313913.1:c.572G>T	NP_001300842.1:p.Gly191Val
XM_005262397.3:c.557G>T	XP_005262454.1:p.Gly186Val
XM_005262397.4:c.557G>T	XP_005262454.1:p.Gly186Val
NM_000133.4:c.686G>T MANE Select	NP_000124.1:p.Gly229Val
NM_001313913.2:c.572G>T	NP_001300842.1:p.Gly191Val