Canonical Allele Identifier: CA158648311
Gene:

Linked Data

dbSNP Id: rs966569217
MyVariant Identifiers: chr7:g.50214258C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.50214258C>T , CM000669.2:g.50214258C>T GRCh38
NC_000007.13:g.50253854C>T , CM000669.1:g.50253854C>T GRCh37
NC_000007.12:g.50224400C>T NCBI36