Canonical Allele Identifier: CA414440225

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138633221T>C (hg19) ; chrX:g.139551062T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551062T>C , CM000685.2:g.139551062T>C	GRCh38
NC_000023.10:g.138633221T>C , CM000685.1:g.138633221T>C	GRCh37
NC_000023.9:g.138460887T>C	NCBI36
NG_007994.1:g.25327T>C , LRG_556:g.25327T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.521T>C MANE Select	ENSP00000218099.2:p.Val174Ala
ENST00000643157.1:n.1188T>C
ENST00000218099.6:c.521T>C	ENSP00000218099.2:p.Val174Ala
ENST00000394090.2:c.407T>C	ENSP00000377650.2:p.Val136Ala
NM_000133.3:c.521T>C , LRG_556t1:c.521T>C	NP_000124.1:p.Val174Ala
NM_001313913.1:c.407T>C	NP_001300842.1:p.Val136Ala
XM_005262397.3:c.392T>C	XP_005262454.1:p.Val131Ala
XM_005262397.4:c.392T>C	XP_005262454.1:p.Val131Ala
NM_000133.4:c.521T>C MANE Select	NP_000124.1:p.Val174Ala
NM_001313913.2:c.407T>C	NP_001300842.1:p.Val136Ala