Canonical Allele Identifier: CA1407372291

Gene: SLC9A9

Linked Data

• dbSNP Id: rs2031961567

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337432C>A , CM000665.2:g.143337432C>A	GRCh38
NC_000003.11:g.143056274C>A , CM000665.1:g.143056274C>A	GRCh37
NC_000003.10:g.144538964C>A	NCBI36
NG_017077.1:g.516100G>T
NG_017077.2:g.516100G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1604+26052G>T MANE Select	ENSP00000320246.6:n.1604+26052G>T
ENST00000316549.10:c.1604+26052G>T	ENSP00000320246.6:n.1604+26052G>T
NM_173653.3:c.1604+26052G>T	NP_775924.1:n.1604+26052G>T
XM_011512703.1:c.956+26052G>T	XP_011511005.1:n.956+26052G>T
XM_011512703.3:c.956+26052G>T	XP_011511005.1:n.956+26052G>T
XM_017006202.2:c.1711+25945G>T	XP_016861691.1:n.1711+25945G>T
XM_017006203.1:c.1253+26052G>T	XP_016861692.1:n.1253+26052G>T
NM_173653.4:c.1604+26052G>T MANE Select	NP_775924.1:n.1604+26052G>T