Canonical Allele Identifier: CA85222844

Gene: SLC9A9

Linked Data

• dbSNP Id: rs139881216
• gnomAD v2: 3-143056447-T-A
• gnomAD v3: 3-143337605-T-A
• gnomAD v4: 3-143337605-T-A
• MyVariant Identifiers: chr3:g.143056447T>A (hg19) ; chr3:g.143337605T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143337605T>A , CM000665.2:g.143337605T>A	GRCh38
NC_000003.11:g.143056447T>A , CM000665.1:g.143056447T>A	GRCh37
NC_000003.10:g.144539137T>A	NCBI36
NG_017077.1:g.515927A>T
NG_017077.2:g.515927A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.1604+25879A>T MANE Select	ENSP00000320246.6:n.1604+25879A>T
ENST00000316549.10:c.1604+25879A>T	ENSP00000320246.6:n.1604+25879A>T
NM_173653.3:c.1604+25879A>T	NP_775924.1:n.1604+25879A>T
XM_011512703.1:c.956+25879A>T	XP_011511005.1:n.956+25879A>T
XM_011512703.3:c.956+25879A>T	XP_011511005.1:n.956+25879A>T
XM_017006202.2:c.1711+25772A>T	XP_016861691.1:n.1711+25772A>T
XM_017006203.1:c.1253+25879A>T	XP_016861692.1:n.1253+25879A>T
NM_173653.4:c.1604+25879A>T MANE Select	NP_775924.1:n.1604+25879A>T