Canonical Allele Identifier: CA871867880

Gene: SLC9A6

Linked Data

• dbSNP Id: rs1218458813
• MyVariant Identifiers: chrX:g.135985322A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.135985322A>T , CM000685.2:g.135985322A>T	GRCh38
NC_000023.10:g.135067481A>T , CM000685.1:g.135067481A>T	GRCh37
NC_000023.9:g.134895147A>T	NCBI36
NG_017160.1:g.4896A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370701.6:c.-212A>T	ENSP00000359735.1:n.-212A>T
ENST00000636092.1:c.-56-281A>T	ENSP00000490406.1:n.-56-281A>T
ENST00000636347.1:c.-35-302A>T	ENSP00000490648.1:n.-35-302A>T
ENST00000637195.1:c.-35-302A>T	ENSP00000490330.1:n.-35-302A>T
ENST00000637234.1:c.-56-281A>T	ENSP00000490527.1:n.-56-281A>T
ENST00000637581.1:c.-56-281A>T	ENSP00000490731.1:n.-56-281A>T
XM_006724726.3:c.-207A>T	XP_006724789.1:n.-207A>T
XM_017029223.2:c.-56-281A>T	XP_016884712.1:n.-56-281A>T
XM_017029224.1:c.-56-281A>T	XP_016884713.1:n.-56-281A>T
NM_001400909.1:c.-35-302A>T	NP_001387838.1:n.-35-302A>T
NM_001400910.1:c.-56-281A>T	NP_001387839.1:n.-56-281A>T
NM_001400911.1:c.-56-281A>T	NP_001387840.1:n.-56-281A>T