Linked Data
dbSNP Id:
rs149212747
MyVariant Identifiers:
chr12:g.111836771_111836772insCC (hg19)
chr12:g.111398967_111398968insCC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.111398973_111398974dup , CM000674.2:g.111398973_111398974dup | GRCh38 |
| NC_000012.11:g.111836777_111836778dup , CM000674.1:g.111836777_111836778dup | GRCh37 |
| NC_000012.10:g.110321160_110321161dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_945342.1:n.44+2100_44+2101dup |