Canonical Allele Identifier: CA427841290
Gene: SLC9A4 HGNC NCBI

Linked Data

dbSNP Id: rs1243715695
gnomAD v2: 2-103149021-G-A
gnomAD v4: 2-102532562-G-A
MyVariant Identifiers: chr2:g.103149021G>A (hg19) chr2:g.102532562G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532562G>A , CM000664.2:g.102532562G>A GRCh38
NC_000002.11:g.103149021G>A , CM000664.1:g.103149021G>A GRCh37
NC_000002.10:g.102515453G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000295269.5:c.2271G>A MANE Select ENSP00000295269.4:p.Glu757=
ENST00000295269.4:c.2271G>A ENSP00000295269.4:p.Glu757=
NM_001011552.3:c.2271G>A NP_001011552.2:p.Glu757=
XM_011511158.1:c.2184G>A XP_011509460.1:p.Glu728=
NM_001011552.4:c.2271G>A MANE Select NP_001011552.2:p.Glu757=
Search 100 bp 5'
Search 100 bp 3'