Canonical Allele Identifier: CA871867897

Gene: SLC9A6

Linked Data

• dbSNP Id: rs1344191486
• MyVariant Identifiers: chrX:g.135985371C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985371C>T , CM000685.2:g.135985371C>T	GRCh38
NC_000023.10:g.135067530C>T , CM000685.1:g.135067530C>T	GRCh37
NC_000023.9:g.134895196C>T	NCBI36
NG_017160.1:g.4945C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-163C>T	ENSP00000359735.1:n.-163C>T
ENST00000636092.1:c.-56-232C>T	ENSP00000490406.1:n.-56-232C>T
ENST00000636347.1:c.-35-253C>T	ENSP00000490648.1:n.-35-253C>T
ENST00000637195.1:c.-35-253C>T	ENSP00000490330.1:n.-35-253C>T
ENST00000637234.1:c.-56-232C>T	ENSP00000490527.1:n.-56-232C>T
ENST00000637581.1:c.-56-232C>T	ENSP00000490731.1:n.-56-232C>T
XM_006724726.3:c.-158C>T	XP_006724789.1:n.-158C>T
XM_017029223.2:c.-56-232C>T	XP_016884712.1:n.-56-232C>T
XM_017029224.1:c.-56-232C>T	XP_016884713.1:n.-56-232C>T
NM_001400909.1:c.-35-253C>T	NP_001387838.1:n.-35-253C>T
NM_001400910.1:c.-56-232C>T	NP_001387839.1:n.-56-232C>T
NM_001400911.1:c.-56-232C>T	NP_001387840.1:n.-56-232C>T