Canonical Allele Identifier: CA347952008
Gene: SLC9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.103149015T>A (hg19) chr2:g.102532556T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532556T>A , CM000664.2:g.102532556T>A GRCh38
NC_000002.11:g.103149015T>A , CM000664.1:g.103149015T>A GRCh37
NC_000002.10:g.102515447T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000295269.5:c.2265T>A MANE Select ENSP00000295269.4:p.Asp755Glu
ENST00000295269.4:c.2265T>A ENSP00000295269.4:p.Asp755Glu
NM_001011552.3:c.2265T>A NP_001011552.2:p.Asp755Glu
XM_011511158.1:c.2178T>A XP_011509460.1:p.Asp726Glu
NM_001011552.4:c.2265T>A MANE Select NP_001011552.2:p.Asp755Glu
Search 100 bp 5'
Search 100 bp 3'