Canonical Allele Identifier: CA334701379
Gene:

Linked Data

dbSNP Id: rs1001621160
MyVariant Identifiers: chrX:g.115688196G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.115688196G>A , CM000685.2:g.115688196G>A GRCh38
NC_000023.10:g.114922516G>A , CM000685.1:g.114922516G>A GRCh37
NC_000023.9:g.114828772G>A NCBI36