Canonical Allele Identifier: CA191124872
Gene: SLC24A2 HGNC NCBI

Linked Data

dbSNP Id: rs978191694
gnomAD v2: 9-20145776-C-A
gnomAD v3: 9-20145778-C-A
gnomAD v4: 9-20145778-C-A
MyVariant Identifiers: chr9:g.20145776C>A (hg19) chr9:g.20145778C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.20145778C>A , CM000671.2:g.20145778C>A GRCh38
NC_000009.11:g.20145776C>A , CM000671.1:g.20145776C>A GRCh37
NC_000009.10:g.20135776C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014592.1:c.-528-141391G>T XP_016870081.1:n.-528-141391G>T
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