Canonical Allele Identifier: CA85301835
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs995976757

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143707124A>G , CM000665.2:g.143707124A>G GRCh38
NC_000003.11:g.143425966A>G , CM000665.1:g.143425966A>G GRCh37
NC_000003.10:g.144908656A>G NCBI36
NG_017077.1:g.146408T>C
NG_017077.2:g.146408T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.534-13817T>C MANE Select ENSP00000320246.6:n.534-13817T>C
ENST00000316549.10:c.534-13817T>C ENSP00000320246.6:n.534-13817T>C
ENST00000474727.2:c.*145-13817T>C ENSP00000419090.2:n.*145-13817T>C
NM_173653.3:c.534-13817T>C NP_775924.1:n.534-13817T>C
XM_011512704.1:c.534-13817T>C XP_011511006.1:n.534-13817T>C
XM_011512704.3:c.534-13817T>C XP_011511006.1:n.534-13817T>C
XM_017006202.2:c.534-13817T>C XP_016861691.1:n.534-13817T>C
XM_017006203.1:c.183-13817T>C XP_016861692.1:n.183-13817T>C
NM_173653.4:c.534-13817T>C MANE Select NP_775924.1:n.534-13817T>C