Canonical Allele Identifier: CA900031133
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1206943908
MyVariant Identifiers: chr3:g.143424728T>C (hg19) chr3:g.143705886T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143705886T>C , CM000665.2:g.143705886T>C GRCh38
NC_000003.11:g.143424728T>C , CM000665.1:g.143424728T>C GRCh37
NC_000003.10:g.144907418T>C NCBI36
NG_017077.1:g.147646A>G
NG_017077.2:g.147646A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.534-12579A>G MANE Select ENSP00000320246.6:n.534-12579A>G
ENST00000316549.10:c.534-12579A>G ENSP00000320246.6:n.534-12579A>G
ENST00000474727.2:c.*145-12579A>G ENSP00000419090.2:n.*145-12579A>G
NM_173653.3:c.534-12579A>G NP_775924.1:n.534-12579A>G
XM_011512704.1:c.534-12579A>G XP_011511006.1:n.534-12579A>G
XM_011512704.3:c.534-12579A>G XP_011511006.1:n.534-12579A>G
XM_017006202.2:c.534-12579A>G XP_016861691.1:n.534-12579A>G
XM_017006203.1:c.183-12579A>G XP_016861692.1:n.183-12579A>G
NM_173653.4:c.534-12579A>G MANE Select NP_775924.1:n.534-12579A>G
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