Canonical Allele Identifier: CA223605999
Gene: SLC3A2 HGNC NCBI

Linked Data

dbSNP Id: rs1050950295
gnomAD v2: 11-62623483-G-A
gnomAD v3: 11-62856011-G-A
gnomAD v4: 11-62856011-G-A
MyVariant Identifiers: chr11:g.62623483G>A (hg19) chr11:g.62856011G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62856011G>A , CM000673.2:g.62856011G>A GRCh38
NC_000011.9:g.62623483G>A , CM000673.1:g.62623483G>A GRCh37
NC_000011.8:g.62380059G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000680002.1:c.-259G>A ENSP00000506366.1:n.-259G>A
ENST00000680729.1:c.-259G>A ENSP00000505639.1:n.-259G>A
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