Canonical Allele Identifier: CA85310820
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs981486010
MyVariant Identifiers: chr3:g.143504372A>T (hg19) chr3:g.143785530A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143785530A>T , CM000665.2:g.143785530A>T GRCh38
NC_000003.11:g.143504372A>T , CM000665.1:g.143504372A>T GRCh37
NC_000003.10:g.144987062A>T NCBI36
NG_017077.1:g.68002T>A
NG_017077.2:g.68002T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.533+9471T>A MANE Select ENSP00000320246.6:n.533+9471T>A
ENST00000316549.10:c.533+9471T>A ENSP00000320246.6:n.533+9471T>A
ENST00000474727.2:c.*144+9471T>A ENSP00000419090.2:n.*144+9471T>A
NM_173653.3:c.533+9471T>A NP_775924.1:n.533+9471T>A
XM_011512704.1:c.533+9471T>A XP_011511006.1:n.533+9471T>A
XM_011512704.3:c.533+9471T>A XP_011511006.1:n.533+9471T>A
XM_017006202.2:c.533+9471T>A XP_016861691.1:n.533+9471T>A
XM_017006203.1:c.182+9471T>A XP_016861692.1:n.182+9471T>A
NM_173653.4:c.533+9471T>A MANE Select NP_775924.1:n.533+9471T>A
Search 100 bp 5'
Search 100 bp 3'