Canonical Allele Identifier: CA85214782
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs1008145329
MyVariant Identifiers: chr3:g.143020776C>T (hg19) chr3:g.143301934C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143301934C>T , CM000665.2:g.143301934C>T GRCh38
NC_000003.11:g.143020776C>T , CM000665.1:g.143020776C>T GRCh37
NC_000003.10:g.144503466C>T NCBI36
NG_017077.1:g.551598G>A
NG_017077.2:g.551598G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.1605-32954G>A MANE Select ENSP00000320246.6:n.1605-32954G>A
ENST00000316549.10:c.1605-32954G>A ENSP00000320246.6:n.1605-32954G>A
NM_173653.3:c.1605-32954G>A NP_775924.1:n.1605-32954G>A
XM_011512703.1:c.957-32954G>A XP_011511005.1:n.957-32954G>A
XM_011512703.3:c.957-32954G>A XP_011511005.1:n.957-32954G>A
XM_017006202.2:c.1712-17592G>A XP_016861691.1:n.1712-17592G>A
XM_017006203.1:c.1254-32954G>A XP_016861692.1:n.1254-32954G>A
NM_173653.4:c.1605-32954G>A MANE Select NP_775924.1:n.1605-32954G>A
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