Canonical Allele Identifier: CA85301844

Gene: SLC9A9

Linked Data

• dbSNP Id: rs556363843
• gnomAD v3: 3-143707189-C-G
• gnomAD v4: 3-143707189-C-G
• MyVariant Identifiers: chr3:g.143426031C>G (hg19) ; chr3:g.143707189C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143707189C>G , CM000665.2:g.143707189C>G	GRCh38
NC_000003.11:g.143426031C>G , CM000665.1:g.143426031C>G	GRCh37
NC_000003.10:g.144908721C>G	NCBI36
NG_017077.1:g.146343G>C
NG_017077.2:g.146343G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.534-13882G>C MANE Select	ENSP00000320246.6:n.534-13882G>C
ENST00000316549.10:c.534-13882G>C	ENSP00000320246.6:n.534-13882G>C
ENST00000474727.2:c.*145-13882G>C	ENSP00000419090.2:n.*145-13882G>C
NM_173653.3:c.534-13882G>C	NP_775924.1:n.534-13882G>C
XM_011512704.1:c.534-13882G>C	XP_011511006.1:n.534-13882G>C
XM_011512704.3:c.534-13882G>C	XP_011511006.1:n.534-13882G>C
XM_017006202.2:c.534-13882G>C	XP_016861691.1:n.534-13882G>C
XM_017006203.1:c.183-13882G>C	XP_016861692.1:n.183-13882G>C
NM_173653.4:c.534-13882G>C MANE Select	NP_775924.1:n.534-13882G>C