Canonical Allele Identifier: CA414445462

Gene: F9

Linked Data

• dbSNP Id: rs1928111815
• MyVariant Identifiers: chrX:g.138643872A>G (hg19) ; chrX:g.139561713A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561713A>G , CM000685.2:g.139561713A>G	GRCh38
NC_000023.10:g.138643872A>G , CM000685.1:g.138643872A>G	GRCh37
NC_000023.9:g.138471538A>G	NCBI36
NG_007994.1:g.35978A>G , LRG_556:g.35978A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.1028A>G MANE Select	ENSP00000218099.2:p.Asn343Ser
ENST00000643157.1:n.1695A>G
ENST00000218099.6:c.1028A>G	ENSP00000218099.2:p.Asn343Ser
ENST00000394090.2:c.914A>G	ENSP00000377650.2:p.Asn305Ser
NM_000133.3:c.1028A>G , LRG_556t1:c.1028A>G	NP_000124.1:p.Asn343Ser
NM_001313913.1:c.914A>G	NP_001300842.1:p.Asn305Ser
XM_005262397.3:c.899A>G	XP_005262454.1:p.Asn300Ser
XM_005262397.4:c.899A>G	XP_005262454.1:p.Asn300Ser
NM_000133.4:c.1028A>G MANE Select	NP_000124.1:p.Asn343Ser
NM_001313913.2:c.914A>G	NP_001300842.1:p.Asn305Ser