Canonical Allele Identifier: CA191124841
Gene: SLC24A2 HGNC NCBI

Linked Data

dbSNP Id: rs151128157
gnomAD v2: 9-20145618-T-C
gnomAD v3: 9-20145620-T-C
gnomAD v4: 9-20145620-T-C
MyVariant Identifiers: chr9:g.20145618T>C (hg19) chr9:g.20145620T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.20145620T>C , CM000671.2:g.20145620T>C GRCh38
NC_000009.11:g.20145618T>C , CM000671.1:g.20145618T>C GRCh37
NC_000009.10:g.20135618T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014592.1:c.-528-141233A>G XP_016870081.1:n.-528-141233A>G
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