Canonical Allele Identifier: CA85222834

Gene: SLC9A9

Linked Data

• dbSNP Id: rs564441105
• gnomAD v3: 3-143337543-T-C
• gnomAD v4: 3-143337543-T-C
• MyVariant Identifiers: chr3:g.143056385T>C (hg19) ; chr3:g.143337543T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337543T>C , CM000665.2:g.143337543T>C	GRCh38
NC_000003.11:g.143056385T>C , CM000665.1:g.143056385T>C	GRCh37
NC_000003.10:g.144539075T>C	NCBI36
NG_017077.1:g.515989A>G
NG_017077.2:g.515989A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1604+25941A>G MANE Select	ENSP00000320246.6:n.1604+25941A>G
ENST00000316549.10:c.1604+25941A>G	ENSP00000320246.6:n.1604+25941A>G
NM_173653.3:c.1604+25941A>G	NP_775924.1:n.1604+25941A>G
XM_011512703.1:c.956+25941A>G	XP_011511005.1:n.956+25941A>G
XM_011512703.3:c.956+25941A>G	XP_011511005.1:n.956+25941A>G
XM_017006202.2:c.1711+25834A>G	XP_016861691.1:n.1711+25834A>G
XM_017006203.1:c.1253+25941A>G	XP_016861692.1:n.1253+25941A>G
NM_173653.4:c.1604+25941A>G MANE Select	NP_775924.1:n.1604+25941A>G