Canonical Allele Identifier: CA12016995
Gene:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172767870C>T , CM000667.2:g.172767870C>T GRCh38
NC_000005.9:g.172194873C>T , CM000667.1:g.172194873C>T GRCh37
NC_000005.8:g.172127478C>T NCBI36