Canonical Allele Identifier: CA2460185261

Gene: SLC9A6

Linked Data

• dbSNP Id: rs1556614628
• gnomAD v4: X-135985346-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985346G>C , CM000685.2:g.135985346G>C	GRCh38
NC_000023.10:g.135067505G>C , CM000685.1:g.135067505G>C	GRCh37
NC_000023.9:g.134895171G>C	NCBI36
NG_017160.1:g.4920G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-188G>C	ENSP00000359735.1:n.-188G>C
ENST00000636092.1:c.-56-257G>C	ENSP00000490406.1:n.-56-257G>C
ENST00000636347.1:c.-35-278G>C	ENSP00000490648.1:n.-35-278G>C
ENST00000637195.1:c.-35-278G>C	ENSP00000490330.1:n.-35-278G>C
ENST00000637234.1:c.-56-257G>C	ENSP00000490527.1:n.-56-257G>C
ENST00000637581.1:c.-56-257G>C	ENSP00000490731.1:n.-56-257G>C
XM_006724726.3:c.-183G>C	XP_006724789.1:n.-183G>C
XM_017029223.2:c.-56-257G>C	XP_016884712.1:n.-56-257G>C
XM_017029224.1:c.-56-257G>C	XP_016884713.1:n.-56-257G>C
NM_001400909.1:c.-35-278G>C	NP_001387838.1:n.-35-278G>C
NM_001400910.1:c.-56-257G>C	NP_001387839.1:n.-56-257G>C
NM_001400911.1:c.-56-257G>C	NP_001387840.1:n.-56-257G>C