Canonical Allele Identifier: CA899976728

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1474385323
• gnomAD v3: 3-143337741-A-G
• gnomAD v4: 3-143337741-A-G
• MyVariant Identifiers: chr3:g.143056583A>G (hg19) ; chr3:g.143337741A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337741A>G , CM000665.2:g.143337741A>G	GRCh38
NC_000003.11:g.143056583A>G , CM000665.1:g.143056583A>G	GRCh37
NC_000003.10:g.144539273A>G	NCBI36
NG_017077.1:g.515791T>C
NG_017077.2:g.515791T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.1604+25743T>C MANE Select	ENSP00000320246.6:n.1604+25743T>C
ENST00000316549.10:c.1604+25743T>C	ENSP00000320246.6:n.1604+25743T>C
NM_173653.3:c.1604+25743T>C	NP_775924.1:n.1604+25743T>C
XM_011512703.1:c.956+25743T>C	XP_011511005.1:n.956+25743T>C
XM_011512703.3:c.956+25743T>C	XP_011511005.1:n.956+25743T>C
XM_017006202.2:c.1711+25636T>C	XP_016861691.1:n.1711+25636T>C
XM_017006203.1:c.1253+25743T>C	XP_016861692.1:n.1253+25743T>C
NM_173653.4:c.1604+25743T>C MANE Select	NP_775924.1:n.1604+25743T>C