Canonical Allele Identifier: CA861971671
Gene: SLC24A2 HGNC NCBI

Linked Data

dbSNP Id: rs1389996377
gnomAD v3: 9-20145512-A-AT
gnomAD v4: 9-20145512-A-AT
MyVariant Identifiers: chr9:g.20145510_20145511insT (hg19) chr9:g.20145512_20145513insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.20145516dup , CM000671.2:g.20145516dup GRCh38
NC_000009.11:g.20145514dup , CM000671.1:g.20145514dup GRCh37
NC_000009.10:g.20135514dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014592.1:c.-528-141126dup XP_016870081.1:n.-528-141126dup
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