Canonical Allele Identifier: CA518862064

Gene: F9

Linked Data

• MyVariant Identifiers: chrX:g.138633345T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551186T>C , CM000685.2:g.139551186T>C	GRCh38
NC_000023.10:g.138633345T>C , CM000685.1:g.138633345T>C	GRCh37
NC_000023.9:g.138461011T>C	NCBI36
NG_007994.1:g.25451T>C , LRG_556:g.25451T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.645T>C MANE Select	ENSP00000218099.2:p.Thr215=
ENST00000643157.1:n.1312T>C
ENST00000218099.6:c.645T>C	ENSP00000218099.2:p.Thr215=
ENST00000394090.2:c.531T>C	ENSP00000377650.2:p.Thr177=
NM_000133.3:c.645T>C , LRG_556t1:c.645T>C	NP_000124.1:p.Thr215=
NM_001313913.1:c.531T>C	NP_001300842.1:p.Thr177=
XM_005262397.3:c.516T>C	XP_005262454.1:p.Thr172=
XM_005262397.4:c.516T>C	XP_005262454.1:p.Thr172=
NM_000133.4:c.645T>C MANE Select	NP_000124.1:p.Thr215=
NM_001313913.2:c.531T>C	NP_001300842.1:p.Thr177=