Canonical Allele Identifier: CA899976536

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1167804972
• gnomAD v3: 3-143337471-A-G
• gnomAD v4: 3-143337471-A-G
• MyVariant Identifiers: chr3:g.143056313A>G (hg19) ; chr3:g.143337471A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337471A>G , CM000665.2:g.143337471A>G	GRCh38
NC_000003.11:g.143056313A>G , CM000665.1:g.143056313A>G	GRCh37
NC_000003.10:g.144539003A>G	NCBI36
NG_017077.1:g.516061T>C
NG_017077.2:g.516061T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1604+26013T>C MANE Select	ENSP00000320246.6:n.1604+26013T>C
ENST00000316549.10:c.1604+26013T>C	ENSP00000320246.6:n.1604+26013T>C
NM_173653.3:c.1604+26013T>C	NP_775924.1:n.1604+26013T>C
XM_011512703.1:c.956+26013T>C	XP_011511005.1:n.956+26013T>C
XM_011512703.3:c.956+26013T>C	XP_011511005.1:n.956+26013T>C
XM_017006202.2:c.1711+25906T>C	XP_016861691.1:n.1711+25906T>C
XM_017006203.1:c.1253+26013T>C	XP_016861692.1:n.1253+26013T>C
NM_173653.4:c.1604+26013T>C MANE Select	NP_775924.1:n.1604+26013T>C