Canonical Allele Identifier: CA85211205
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs17636071

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143286187T>C , CM000665.2:g.143286187T>C GRCh38
NC_000003.11:g.143005029T>C , CM000665.1:g.143005029T>C GRCh37
NC_000003.10:g.144487719T>C NCBI36
NG_017077.1:g.567345A>G
NG_017077.2:g.567345A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.1605-17207A>G MANE Select ENSP00000320246.6:n.1605-17207A>G
ENST00000316549.10:c.1605-17207A>G ENSP00000320246.6:n.1605-17207A>G
NM_173653.3:c.1605-17207A>G NP_775924.1:n.1605-17207A>G
XM_011512703.1:c.957-17207A>G XP_011511005.1:n.957-17207A>G
XM_011512703.3:c.957-17207A>G XP_011511005.1:n.957-17207A>G
XM_017006202.2:c.1712-1845A>G XP_016861691.1:n.1712-1845A>G
XM_017006203.1:c.1254-17207A>G XP_016861692.1:n.1254-17207A>G
NM_173653.4:c.1605-17207A>G MANE Select NP_775924.1:n.1605-17207A>G