Canonical Allele Identifier: CA899999756

Gene: SLC9A9

Linked Data

• dbSNP Id: rs1286719384
• MyVariant Identifiers: chr3:g.143020810G>A (hg19) ; chr3:g.143301968G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.143301968G>A , CM000665.2:g.143301968G>A	GRCh38
NC_000003.11:g.143020810G>A , CM000665.1:g.143020810G>A	GRCh37
NC_000003.10:g.144503500G>A	NCBI36
NG_017077.1:g.551564C>T
NG_017077.2:g.551564C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000316549.11:c.1605-32988C>T MANE Select	ENSP00000320246.6:n.1605-32988C>T
ENST00000316549.10:c.1605-32988C>T	ENSP00000320246.6:n.1605-32988C>T
NM_173653.3:c.1605-32988C>T	NP_775924.1:n.1605-32988C>T
XM_011512703.1:c.957-32988C>T	XP_011511005.1:n.957-32988C>T
XM_011512703.3:c.957-32988C>T	XP_011511005.1:n.957-32988C>T
XM_017006202.2:c.1712-17626C>T	XP_016861691.1:n.1712-17626C>T
XM_017006203.1:c.1254-32988C>T	XP_016861692.1:n.1254-32988C>T
NM_173653.4:c.1605-32988C>T MANE Select	NP_775924.1:n.1605-32988C>T