Canonical Allele Identifier: CA191124826
Gene: SLC24A2 HGNC NCBI

Linked Data

dbSNP Id: rs977866078
MyVariant Identifiers: chr9:g.20145461G>C (hg19) chr9:g.20145463G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.20145463G>C , CM000671.2:g.20145463G>C GRCh38
NC_000009.11:g.20145461G>C , CM000671.1:g.20145461G>C GRCh37
NC_000009.10:g.20135461G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014592.1:c.-528-141076C>G XP_016870081.1:n.-528-141076C>G
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