Canonical Allele Identifier: CA899999801

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1327611760
• gnomAD v3: 3-143302076-C-T
• gnomAD v4: 3-143302076-C-T
• MyVariant Identifiers: chr3:g.143020918C>T (hg19) ; chr3:g.143302076C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143302076C>T , CM000665.2:g.143302076C>T	GRCh38
NC_000003.11:g.143020918C>T , CM000665.1:g.143020918C>T	GRCh37
NC_000003.10:g.144503608C>T	NCBI36
NG_017077.1:g.551456G>A
NG_017077.2:g.551456G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.1605-33096G>A MANE Select	ENSP00000320246.6:n.1605-33096G>A
ENST00000316549.10:c.1605-33096G>A	ENSP00000320246.6:n.1605-33096G>A
NM_173653.3:c.1605-33096G>A	NP_775924.1:n.1605-33096G>A
XM_011512703.1:c.957-33096G>A	XP_011511005.1:n.957-33096G>A
XM_011512703.3:c.957-33096G>A	XP_011511005.1:n.957-33096G>A
XM_017006202.2:c.1712-17734G>A	XP_016861691.1:n.1712-17734G>A
XM_017006203.1:c.1254-33096G>A	XP_016861692.1:n.1254-33096G>A
NM_173653.4:c.1605-33096G>A MANE Select	NP_775924.1:n.1605-33096G>A