Canonical Allele Identifier: CA191124848
Gene: SLC24A2 HGNC NCBI

Linked Data

dbSNP Id: rs201115728
gnomAD v2: 9-20145630-A-C
gnomAD v3: 9-20145632-A-C
gnomAD v4: 9-20145632-A-C
MyVariant Identifiers: chr9:g.20145630A>C (hg19) chr9:g.20145630_20145631delinsCT (hg19) chr9:g.20145632A>C (hg38) chr9:g.20145632_20145633delinsCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.20145632A>C , CM000671.2:g.20145632A>C GRCh38
NC_000009.11:g.20145630A>C , CM000671.1:g.20145630A>C GRCh37
NC_000009.10:g.20135630A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014592.1:c.-528-141245T>G XP_016870081.1:n.-528-141245T>G
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