Canonical Allele Identifier: CA10529871

Gene: F9

Linked Data

• dbSNP Id: rs750955240
• ExAC: X:138643951 T / C
• gnomAD v2: X-138643951-T-C
• MyVariant Identifiers: chrX:g.138643951T>C (hg19) ; chrX:g.139561792T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561792T>C , CM000685.2:g.139561792T>C	GRCh38
NC_000023.10:g.138643951T>C , CM000685.1:g.138643951T>C	GRCh37
NC_000023.9:g.138471617T>C	NCBI36
NG_007994.1:g.36057T>C , LRG_556:g.36057T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1107T>C MANE Select	ENSP00000218099.2:p.Leu369=
ENST00000643157.1:n.1723+51T>C
ENST00000218099.6:c.1107T>C	ENSP00000218099.2:p.Leu369=
ENST00000394090.2:c.993T>C	ENSP00000377650.2:p.Leu331=
NM_000133.3:c.1107T>C , LRG_556t1:c.1107T>C	NP_000124.1:p.Leu369=
NM_001313913.1:c.993T>C	NP_001300842.1:p.Leu331=
XM_005262397.3:c.978T>C	XP_005262454.1:p.Leu326=
XM_005262397.4:c.978T>C	XP_005262454.1:p.Leu326=
NM_000133.4:c.1107T>C MANE Select	NP_000124.1:p.Leu369=
NM_001313913.2:c.993T>C	NP_001300842.1:p.Leu331=