Canonical Allele Identifier: CA85222849

Gene: SLC9A9

Linked Data

• dbSNP Id: rs887973562
• MyVariant Identifiers: chr3:g.143056485A>T (hg19) ; chr3:g.143337643A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337643A>T , CM000665.2:g.143337643A>T	GRCh38
NC_000003.11:g.143056485A>T , CM000665.1:g.143056485A>T	GRCh37
NC_000003.10:g.144539175A>T	NCBI36
NG_017077.1:g.515889T>A
NG_017077.2:g.515889T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.1604+25841T>A MANE Select	ENSP00000320246.6:n.1604+25841T>A
ENST00000316549.10:c.1604+25841T>A	ENSP00000320246.6:n.1604+25841T>A
NM_173653.3:c.1604+25841T>A	NP_775924.1:n.1604+25841T>A
XM_011512703.1:c.956+25841T>A	XP_011511005.1:n.956+25841T>A
XM_011512703.3:c.956+25841T>A	XP_011511005.1:n.956+25841T>A
XM_017006202.2:c.1711+25734T>A	XP_016861691.1:n.1711+25734T>A
XM_017006203.1:c.1253+25841T>A	XP_016861692.1:n.1253+25841T>A
NM_173653.4:c.1604+25841T>A MANE Select	NP_775924.1:n.1604+25841T>A