Canonical Allele Identifier: CA900031159
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1382389237
MyVariant Identifiers: chr3:g.143424760T>G (hg19) chr3:g.143705918T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143705918T>G , CM000665.2:g.143705918T>G GRCh38
NC_000003.11:g.143424760T>G , CM000665.1:g.143424760T>G GRCh37
NC_000003.10:g.144907450T>G NCBI36
NG_017077.1:g.147614A>C
NG_017077.2:g.147614A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.534-12611A>C MANE Select ENSP00000320246.6:n.534-12611A>C
ENST00000316549.10:c.534-12611A>C ENSP00000320246.6:n.534-12611A>C
ENST00000474727.2:c.*145-12611A>C ENSP00000419090.2:n.*145-12611A>C
NM_173653.3:c.534-12611A>C NP_775924.1:n.534-12611A>C
XM_011512704.1:c.534-12611A>C XP_011511006.1:n.534-12611A>C
XM_011512704.3:c.534-12611A>C XP_011511006.1:n.534-12611A>C
XM_017006202.2:c.534-12611A>C XP_016861691.1:n.534-12611A>C
XM_017006203.1:c.183-12611A>C XP_016861692.1:n.183-12611A>C
NM_173653.4:c.534-12611A>C MANE Select NP_775924.1:n.534-12611A>C
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