Canonical Allele Identifier: CA899976721

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1190309998
• gnomAD v3: 3-143337733-G-C
• gnomAD v4: 3-143337733-G-C
• MyVariant Identifiers: chr3:g.143056575G>C (hg19) ; chr3:g.143337733G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337733G>C , CM000665.2:g.143337733G>C	GRCh38
NC_000003.11:g.143056575G>C , CM000665.1:g.143056575G>C	GRCh37
NC_000003.10:g.144539265G>C	NCBI36
NG_017077.1:g.515799C>G
NG_017077.2:g.515799C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.1604+25751C>G MANE Select	ENSP00000320246.6:n.1604+25751C>G
ENST00000316549.10:c.1604+25751C>G	ENSP00000320246.6:n.1604+25751C>G
NM_173653.3:c.1604+25751C>G	NP_775924.1:n.1604+25751C>G
XM_011512703.1:c.956+25751C>G	XP_011511005.1:n.956+25751C>G
XM_011512703.3:c.956+25751C>G	XP_011511005.1:n.956+25751C>G
XM_017006202.2:c.1711+25644C>G	XP_016861691.1:n.1711+25644C>G
XM_017006203.1:c.1253+25751C>G	XP_016861692.1:n.1253+25751C>G
NM_173653.4:c.1604+25751C>G MANE Select	NP_775924.1:n.1604+25751C>G