Canonical Allele Identifier: CA85211187
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs969528306
MyVariant Identifiers: chr3:g.143004944T>G (hg19) chr3:g.143286102T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143286102T>G , CM000665.2:g.143286102T>G GRCh38
NC_000003.11:g.143004944T>G , CM000665.1:g.143004944T>G GRCh37
NC_000003.10:g.144487634T>G NCBI36
NG_017077.1:g.567430A>C
NG_017077.2:g.567430A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.1605-17122A>C MANE Select ENSP00000320246.6:n.1605-17122A>C
ENST00000316549.10:c.1605-17122A>C ENSP00000320246.6:n.1605-17122A>C
NM_173653.3:c.1605-17122A>C NP_775924.1:n.1605-17122A>C
XM_011512703.1:c.957-17122A>C XP_011511005.1:n.957-17122A>C
XM_011512703.3:c.957-17122A>C XP_011511005.1:n.957-17122A>C
XM_017006202.2:c.1712-1760A>C XP_016861691.1:n.1712-1760A>C
XM_017006203.1:c.1254-17122A>C XP_016861692.1:n.1254-17122A>C
NM_173653.4:c.1605-17122A>C MANE Select NP_775924.1:n.1605-17122A>C
Search 100 bp 5'
Search 100 bp 3'