Canonical Allele Identifier: CA347952022
Gene: SLC9A4 HGNC NCBI

Linked Data

gnomAD v4: 2-102532562-G-T
MyVariant Identifiers: chr2:g.103149021G>T (hg19) chr2:g.102532562G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000295269.5:c.2271G>T MANE Select ENSP00000295269.4:p.Glu757Asp
ENST00000295269.4:c.2271G>T ENSP00000295269.4:p.Glu757Asp
NM_001011552.3:c.2271G>T NP_001011552.2:p.Glu757Asp
XM_011511158.1:c.2184G>T XP_011509460.1:p.Glu728Asp
NM_001011552.4:c.2271G>T MANE Select NP_001011552.2:p.Glu757Asp
Search 100 bp 5'
Search 100 bp 3'