Canonical Allele Identifier: CA546812297

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1187731978
• gnomAD v2: 3-143056439-G-T
• gnomAD v3: 3-143337597-G-T
• gnomAD v4: 3-143337597-G-T
• MyVariant Identifiers: chr3:g.143056439G>T (hg19) ; chr3:g.143337597G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337597G>T , CM000665.2:g.143337597G>T	GRCh38
NC_000003.11:g.143056439G>T , CM000665.1:g.143056439G>T	GRCh37
NC_000003.10:g.144539129G>T	NCBI36
NG_017077.1:g.515935C>A
NG_017077.2:g.515935C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.1604+25887C>A MANE Select	ENSP00000320246.6:n.1604+25887C>A
ENST00000316549.10:c.1604+25887C>A	ENSP00000320246.6:n.1604+25887C>A
NM_173653.3:c.1604+25887C>A	NP_775924.1:n.1604+25887C>A
XM_011512703.1:c.956+25887C>A	XP_011511005.1:n.956+25887C>A
XM_011512703.3:c.956+25887C>A	XP_011511005.1:n.956+25887C>A
XM_017006202.2:c.1711+25780C>A	XP_016861691.1:n.1711+25780C>A
XM_017006203.1:c.1253+25887C>A	XP_016861692.1:n.1253+25887C>A
NM_173653.4:c.1604+25887C>A MANE Select	NP_775924.1:n.1604+25887C>A