Canonical Allele Identifier: CA191124876
Gene: SLC24A2 HGNC NCBI

Linked Data

dbSNP Id: rs958003091
MyVariant Identifiers: chr9:g.20145787A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.20145787A>T , CM000671.2:g.20145787A>T GRCh38
NC_000009.11:g.20145785A>T , CM000671.1:g.20145785A>T GRCh37
NC_000009.10:g.20135785A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017014592.1:c.-528-141400T>A XP_016870081.1:n.-528-141400T>A