Canonical Allele Identifier: CA1407455233

Gene: SLC9A9

Linked Data

• dbSNP Id: rs2036508570

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143531398T>G , CM000665.2:g.143531398T>G	GRCh38
NC_000003.11:g.143250240T>G , CM000665.1:g.143250240T>G	GRCh37
NC_000003.10:g.144732930T>G	NCBI36
NG_017077.1:g.322134A>C
NG_017077.2:g.322134A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1089+20964A>C MANE Select	ENSP00000320246.6:n.1089+20964A>C
ENST00000316549.10:c.1089+20964A>C	ENSP00000320246.6:n.1089+20964A>C
NM_173653.3:c.1089+20964A>C	NP_775924.1:n.1089+20964A>C
XM_011512703.1:c.441+20964A>C	XP_011511005.1:n.441+20964A>C
XM_011512703.3:c.441+20964A>C	XP_011511005.1:n.441+20964A>C
XM_017006202.2:c.1089+20964A>C	XP_016861691.1:n.1089+20964A>C
XM_017006203.1:c.738+20964A>C	XP_016861692.1:n.738+20964A>C
NM_173653.4:c.1089+20964A>C MANE Select	NP_775924.1:n.1089+20964A>C