Linked Data
dbSNP Id:
rs1282460168
MyVariant Identifiers:
chr2:g.171670915_171670916insCT (hg19)
chr2:g.170814405_170814406insCT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.170814405_170814406insCT , CM000664.2:g.170814405_170814406insCT | GRCh38 |
| NC_000002.11:g.171670915_171670916insCT , CM000664.1:g.171670915_171670916insCT | GRCh37 |
| NC_000002.10:g.171379161_171379162insCT | NCBI36 |
| NG_021477.1:g.2716_2717insCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000454603.5:c.-64+983_-64+984insCT | ENSP00000402366.1:n.-64+983_-64+984insCT | |
| XM_011510922.1:c.-64+983_-64+984insCT | XP_011509224.1:n.-64+983_-64+984insCT |