Canonical Allele Identifier: CA546822010

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1464566988
• gnomAD v2: 3-143250148-C-G
• gnomAD v3: 3-143531306-C-G
• gnomAD v4: 3-143531306-C-G
• MyVariant Identifiers: chr3:g.143250148C>G (hg19) ; chr3:g.143531306C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143531306C>G , CM000665.2:g.143531306C>G	GRCh38
NC_000003.11:g.143250148C>G , CM000665.1:g.143250148C>G	GRCh37
NC_000003.10:g.144732838C>G	NCBI36
NG_017077.1:g.322226G>C
NG_017077.2:g.322226G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316549.11:c.1089+21056G>C MANE Select	ENSP00000320246.6:n.1089+21056G>C
ENST00000316549.10:c.1089+21056G>C	ENSP00000320246.6:n.1089+21056G>C
NM_173653.3:c.1089+21056G>C	NP_775924.1:n.1089+21056G>C
XM_011512703.1:c.441+21056G>C	XP_011511005.1:n.441+21056G>C
XM_011512703.3:c.441+21056G>C	XP_011511005.1:n.441+21056G>C
XM_017006202.2:c.1089+21056G>C	XP_016861691.1:n.1089+21056G>C
XM_017006203.1:c.738+21056G>C	XP_016861692.1:n.738+21056G>C
NM_173653.4:c.1089+21056G>C MANE Select	NP_775924.1:n.1089+21056G>C