Canonical Allele Identifier: CA85301686

Gene: SLC9A9

Linked Data

• dbSNP Id: rs564813026
• gnomAD v3: 3-143705898-A-G
• gnomAD v4: 3-143705898-A-G
• MyVariant Identifiers: chr3:g.143424740A>G (hg19) ; chr3:g.143705898A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143705898A>G , CM000665.2:g.143705898A>G	GRCh38
NC_000003.11:g.143424740A>G , CM000665.1:g.143424740A>G	GRCh37
NC_000003.10:g.144907430A>G	NCBI36
NG_017077.1:g.147634T>C
NG_017077.2:g.147634T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.534-12591T>C MANE Select	ENSP00000320246.6:n.534-12591T>C
ENST00000316549.10:c.534-12591T>C	ENSP00000320246.6:n.534-12591T>C
ENST00000474727.2:c.*145-12591T>C	ENSP00000419090.2:n.*145-12591T>C
NM_173653.3:c.534-12591T>C	NP_775924.1:n.534-12591T>C
XM_011512704.1:c.534-12591T>C	XP_011511006.1:n.534-12591T>C
XM_011512704.3:c.534-12591T>C	XP_011511006.1:n.534-12591T>C
XM_017006202.2:c.534-12591T>C	XP_016861691.1:n.534-12591T>C
XM_017006203.1:c.183-12591T>C	XP_016861692.1:n.183-12591T>C
NM_173653.4:c.534-12591T>C MANE Select	NP_775924.1:n.534-12591T>C