Canonical Allele Identifier: CA48901925
Gene:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.59562570C>T , CM000664.2:g.59562570C>T GRCh38
NC_000002.11:g.59789705C>T , CM000664.1:g.59789705C>T GRCh37
NC_000002.10:g.59643209C>T NCBI36