Canonical Allele Identifier: CA2460185299

Gene: SLC9A6

Linked Data

• dbSNP Id: rs1556614642
• gnomAD v4: X-135985392-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985392C>G , CM000685.2:g.135985392C>G	GRCh38
NC_000023.10:g.135067551C>G , CM000685.1:g.135067551C>G	GRCh37
NC_000023.9:g.134895217C>G	NCBI36
NG_017160.1:g.4966C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-142C>G	ENSP00000359735.1:n.-142C>G
ENST00000636092.1:c.-56-211C>G	ENSP00000490406.1:n.-56-211C>G
ENST00000636347.1:c.-35-232C>G	ENSP00000490648.1:n.-35-232C>G
ENST00000637195.1:c.-35-232C>G	ENSP00000490330.1:n.-35-232C>G
ENST00000637234.1:c.-56-211C>G	ENSP00000490527.1:n.-56-211C>G
ENST00000637581.1:c.-56-211C>G	ENSP00000490731.1:n.-56-211C>G
XM_006724726.3:c.-137C>G	XP_006724789.1:n.-137C>G
XM_017029223.2:c.-56-211C>G	XP_016884712.1:n.-56-211C>G
XM_017029224.1:c.-56-211C>G	XP_016884713.1:n.-56-211C>G
NM_001400909.1:c.-35-232C>G	NP_001387838.1:n.-35-232C>G
NM_001400910.1:c.-56-211C>G	NP_001387839.1:n.-56-211C>G
NM_001400911.1:c.-56-211C>G	NP_001387840.1:n.-56-211C>G