Canonical Allele Identifier: CA347952009
Gene: SLC9A4 HGNC NCBI

Linked Data

gnomAD v4: 2-102532556-T-G
MyVariant Identifiers: chr2:g.103149015T>G (hg19) chr2:g.102532556T>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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