Canonical Allele Identifier: CA1054400482
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1559852540

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143286045T>C , CM000665.2:g.143286045T>C GRCh38
NC_000003.11:g.143004887T>C , CM000665.1:g.143004887T>C GRCh37
NC_000003.10:g.144487577T>C NCBI36
NG_017077.1:g.567487A>G
NG_017077.2:g.567487A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000316549.11:c.1605-17065A>G MANE Select ENSP00000320246.6:n.1605-17065A>G
ENST00000316549.10:c.1605-17065A>G ENSP00000320246.6:n.1605-17065A>G
NM_173653.3:c.1605-17065A>G NP_775924.1:n.1605-17065A>G
XM_011512703.1:c.957-17065A>G XP_011511005.1:n.957-17065A>G
XM_011512703.3:c.957-17065A>G XP_011511005.1:n.957-17065A>G
XM_017006202.2:c.1712-1703A>G XP_016861691.1:n.1712-1703A>G
XM_017006203.1:c.1254-17065A>G XP_016861692.1:n.1254-17065A>G
NM_173653.4:c.1605-17065A>G MANE Select NP_775924.1:n.1605-17065A>G