Canonical Allele Identifier: CA347952012
Gene: SLC9A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.103149017A>C (hg19) chr2:g.102532558A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.102532558A>C , CM000664.2:g.102532558A>C GRCh38
NC_000002.11:g.103149017A>C , CM000664.1:g.103149017A>C GRCh37
NC_000002.10:g.102515449A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000295269.5:c.2267A>C MANE Select ENSP00000295269.4:p.Glu756Ala
ENST00000295269.4:c.2267A>C ENSP00000295269.4:p.Glu756Ala
NM_001011552.3:c.2267A>C NP_001011552.2:p.Glu756Ala
XM_011511158.1:c.2180A>C XP_011509460.1:p.Glu727Ala
NM_001011552.4:c.2267A>C MANE Select NP_001011552.2:p.Glu756Ala
Search 100 bp 5'
Search 100 bp 3'