Canonical Allele Identifier: CA233200098
Gene:

Linked Data

dbSNP Id: rs960437229
MyVariant Identifiers: chr12:g.14260667C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14260667C>G , CM000674.2:g.14260667C>G GRCh38
NC_000012.11:g.14413601C>G , CM000674.1:g.14413601C>G GRCh37
NC_000012.10:g.14304868C>G NCBI36