Canonical Allele Identifier: CA347952006

Gene: SLC9A4

Linked Data

• dbSNP Id: rs1365295717
• gnomAD v3: 2-102532554-G-T
• gnomAD v4: 2-102532554-G-T
• COSMIC: COSM459682
• MyVariant Identifiers: chr2:g.103149013G>T (hg19) ; chr2:g.102532554G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102532554G>T , CM000664.2:g.102532554G>T	GRCh38
NC_000002.11:g.103149013G>T , CM000664.1:g.103149013G>T	GRCh37
NC_000002.10:g.102515445G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295269.5:c.2263G>T MANE Select	ENSP00000295269.4:p.Asp755Tyr
ENST00000295269.4:c.2263G>T	ENSP00000295269.4:p.Asp755Tyr
NM_001011552.3:c.2263G>T	NP_001011552.2:p.Asp755Tyr
XM_011511158.1:c.2176G>T	XP_011509460.1:p.Asp726Tyr
NM_001011552.4:c.2263G>T MANE Select	NP_001011552.2:p.Asp755Tyr