Canonical Allele Identifier: CA414440629

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138633287T>C (hg19) ; chrX:g.139551128T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551128T>C , CM000685.2:g.139551128T>C	GRCh38
NC_000023.10:g.138633287T>C , CM000685.1:g.138633287T>C	GRCh37
NC_000023.9:g.138460953T>C	NCBI36
NG_007994.1:g.25393T>C , LRG_556:g.25393T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.587T>C MANE Select	ENSP00000218099.2:p.Phe196Ser
ENST00000643157.1:n.1254T>C
ENST00000218099.6:c.587T>C	ENSP00000218099.2:p.Phe196Ser
ENST00000394090.2:c.473T>C	ENSP00000377650.2:p.Phe158Ser
NM_000133.3:c.587T>C , LRG_556t1:c.587T>C	NP_000124.1:p.Phe196Ser
NM_001313913.1:c.473T>C	NP_001300842.1:p.Phe158Ser
XM_005262397.3:c.458T>C	XP_005262454.1:p.Phe153Ser
XM_005262397.4:c.458T>C	XP_005262454.1:p.Phe153Ser
NM_000133.4:c.587T>C MANE Select	NP_000124.1:p.Phe196Ser
NM_001313913.2:c.473T>C	NP_001300842.1:p.Phe158Ser