Canonical Allele Identifier: CA869394123
Gene:

Linked Data

dbSNP Id: rs1411644838
MyVariant Identifiers: chrX:g.1029539T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.1029539T>G , CM000685.2:g.1029539T>G GRCh38
NC_000023.10:g.990274T>G , CM000685.1:g.990274T>G GRCh37
NC_000023.9:g.910274T>G NCBI36