Canonical Allele Identifier: CA1407455150

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1210199415

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143531277G>C , CM000665.2:g.143531277G>C	GRCh38
NC_000003.11:g.143250119G>C , CM000665.1:g.143250119G>C	GRCh37
NC_000003.10:g.144732809G>C	NCBI36
NG_017077.1:g.322255C>G
NG_017077.2:g.322255C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1089+21085C>G MANE Select	ENSP00000320246.6:n.1089+21085C>G
ENST00000316549.10:c.1089+21085C>G	ENSP00000320246.6:n.1089+21085C>G
NM_173653.3:c.1089+21085C>G	NP_775924.1:n.1089+21085C>G
XM_011512703.1:c.441+21085C>G	XP_011511005.1:n.441+21085C>G
XM_011512703.3:c.441+21085C>G	XP_011511005.1:n.441+21085C>G
XM_017006202.2:c.1089+21085C>G	XP_016861691.1:n.1089+21085C>G
XM_017006203.1:c.738+21085C>G	XP_016861692.1:n.738+21085C>G
NM_173653.4:c.1089+21085C>G MANE Select	NP_775924.1:n.1089+21085C>G