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Canonical Allele Identifier:
CA869394072
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrX:g.1029445C>T
GRCh37
chrX:g.990180C>T
Linked Data - NCBI & NCI
dbSNP:
4129148
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.1029445C>T , CM000685.2:g.1029445C>T
GRCh38
NC_000023.10:g.990180C>T , CM000685.1:g.990180C>T
GRCh37
NC_000023.9:g.910180C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'