Canonical Allele Identifier: CA223606006
Gene: SLC3A2 HGNC NCBI

Linked Data

dbSNP Id: rs56686759
gnomAD v2: 11-62623497-G-C
gnomAD v3: 11-62856025-G-C
gnomAD v4: 11-62856025-G-C
MyVariant Identifiers: chr11:g.62623497G>C (hg19) chr11:g.62856025G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62856025G>C , CM000673.2:g.62856025G>C GRCh38
NC_000011.9:g.62623497G>C , CM000673.1:g.62623497G>C GRCh37
NC_000011.8:g.62380073G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000680002.1:c.-245G>C ENSP00000506366.1:n.-245G>C
ENST00000680729.1:c.-245G>C ENSP00000505639.1:n.-245G>C
NM_001012662.2:c.-245G>C NP_001012680.1:n.-245G>C
NM_001012664.2:c.-245G>C NP_001012682.1:n.-245G>C
NM_002394.5:c.-245G>C NP_002385.3:n.-245G>C
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