Canonical Allele Identifier: CA336084121

Gene: SLC9A6

Linked Data

• dbSNP Id: rs923909533
• MyVariant Identifiers: chrX:g.135985321G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985321G>C , CM000685.2:g.135985321G>C	GRCh38
NC_000023.10:g.135067480G>C , CM000685.1:g.135067480G>C	GRCh37
NC_000023.9:g.134895146G>C	NCBI36
NG_017160.1:g.4895G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-213G>C	ENSP00000359735.1:n.-213G>C
ENST00000636092.1:c.-56-282G>C	ENSP00000490406.1:n.-56-282G>C
ENST00000636347.1:c.-35-303G>C	ENSP00000490648.1:n.-35-303G>C
ENST00000637195.1:c.-35-303G>C	ENSP00000490330.1:n.-35-303G>C
ENST00000637234.1:c.-56-282G>C	ENSP00000490527.1:n.-56-282G>C
ENST00000637581.1:c.-56-282G>C	ENSP00000490731.1:n.-56-282G>C
XM_006724726.3:c.-208G>C	XP_006724789.1:n.-208G>C
XM_017029223.2:c.-56-282G>C	XP_016884712.1:n.-56-282G>C
XM_017029224.1:c.-56-282G>C	XP_016884713.1:n.-56-282G>C
NM_001400909.1:c.-35-303G>C	NP_001387838.1:n.-35-303G>C
NM_001400910.1:c.-56-282G>C	NP_001387839.1:n.-56-282G>C
NM_001400911.1:c.-56-282G>C	NP_001387840.1:n.-56-282G>C