Canonical Allele Identifier: CA684496005
Gene:

Linked Data

dbSNP Id: rs1243919378
MyVariant Identifiers: chr12:g.121625138C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.121625138C>T , CM000674.2:g.121625138C>T GRCh38
NC_000012.11:g.122063043C>T , CM000674.1:g.122063043C>T GRCh37
NC_000012.10:g.120547426C>T NCBI36
NG_007500.1:g.3569C>T , LRG_93:g.3569C>T