Canonical Allele Identifier: CA85211192
Gene: SLC9A9 HGNC NCBI

Linked Data

dbSNP Id: rs570989122
gnomAD v2: 3-143004951-G-T
gnomAD v3: 3-143286109-G-T
gnomAD v4: 3-143286109-G-T
MyVariant Identifiers: chr3:g.143004951G>T (hg19) chr3:g.143286109G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.143286109G>T , CM000665.2:g.143286109G>T GRCh38
NC_000003.11:g.143004951G>T , CM000665.1:g.143004951G>T GRCh37
NC_000003.10:g.144487641G>T NCBI36
NG_017077.1:g.567423C>A
NG_017077.2:g.567423C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000316549.11:c.1605-17129C>A MANE Select ENSP00000320246.6:n.1605-17129C>A
ENST00000316549.10:c.1605-17129C>A ENSP00000320246.6:n.1605-17129C>A
NM_173653.3:c.1605-17129C>A NP_775924.1:n.1605-17129C>A
XM_011512703.1:c.957-17129C>A XP_011511005.1:n.957-17129C>A
XM_011512703.3:c.957-17129C>A XP_011511005.1:n.957-17129C>A
XM_017006202.2:c.1712-1767C>A XP_016861691.1:n.1712-1767C>A
XM_017006203.1:c.1254-17129C>A XP_016861692.1:n.1254-17129C>A
NM_173653.4:c.1605-17129C>A MANE Select NP_775924.1:n.1605-17129C>A
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