Canonical Allele Identifier: CA587055185
Gene: SLC24A2 HGNC NCBI

Linked Data

dbSNP Id: rs1397569098
gnomAD v2: 9-20145889-T-G
gnomAD v3: 9-20145891-T-G
gnomAD v4: 9-20145891-T-G
MyVariant Identifiers: chr9:g.20145889T>G (hg19) chr9:g.20145891T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.20145891T>G , CM000671.2:g.20145891T>G GRCh38
NC_000009.11:g.20145889T>G , CM000671.1:g.20145889T>G GRCh37
NC_000009.10:g.20135889T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017014592.1:c.-528-141504A>C XP_016870081.1:n.-528-141504A>C
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