Canonical Allele Identifier: CA900065593

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1454719480
• gnomAD v3: 3-143785709-A-G
• gnomAD v4: 3-143785709-A-G
• MyVariant Identifiers: chr3:g.143504551A>G (hg19) ; chr3:g.143785709A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143785709A>G , CM000665.2:g.143785709A>G	GRCh38
NC_000003.11:g.143504551A>G , CM000665.1:g.143504551A>G	GRCh37
NC_000003.10:g.144987241A>G	NCBI36
NG_017077.1:g.67823T>C
NG_017077.2:g.67823T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.533+9292T>C MANE Select	ENSP00000320246.6:n.533+9292T>C
ENST00000316549.10:c.533+9292T>C	ENSP00000320246.6:n.533+9292T>C
ENST00000474727.2:c.*144+9292T>C	ENSP00000419090.2:n.*144+9292T>C
NM_173653.3:c.533+9292T>C	NP_775924.1:n.533+9292T>C
XM_011512704.1:c.533+9292T>C	XP_011511006.1:n.533+9292T>C
XM_011512704.3:c.533+9292T>C	XP_011511006.1:n.533+9292T>C
XM_017006202.2:c.533+9292T>C	XP_016861691.1:n.533+9292T>C
XM_017006203.1:c.182+9292T>C	XP_016861692.1:n.182+9292T>C
NM_173653.4:c.533+9292T>C MANE Select	NP_775924.1:n.533+9292T>C