Canonical Allele Identifier: CA1407354881

Gene: SLC9A9

Linked Data

• dbSNP Id: rs2030544695

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143302031G>C , CM000665.2:g.143302031G>C	GRCh38
NC_000003.11:g.143020873G>C , CM000665.1:g.143020873G>C	GRCh37
NC_000003.10:g.144503563G>C	NCBI36
NG_017077.1:g.551501C>G
NG_017077.2:g.551501C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.1605-33051C>G MANE Select	ENSP00000320246.6:n.1605-33051C>G
ENST00000316549.10:c.1605-33051C>G	ENSP00000320246.6:n.1605-33051C>G
NM_173653.3:c.1605-33051C>G	NP_775924.1:n.1605-33051C>G
XM_011512703.1:c.957-33051C>G	XP_011511005.1:n.957-33051C>G
XM_011512703.3:c.957-33051C>G	XP_011511005.1:n.957-33051C>G
XM_017006202.2:c.1712-17689C>G	XP_016861691.1:n.1712-17689C>G
XM_017006203.1:c.1254-33051C>G	XP_016861692.1:n.1254-33051C>G
NM_173653.4:c.1605-33051C>G MANE Select	NP_775924.1:n.1605-33051C>G