Linked Data
MyVariant Identifiers:
chr2:g.208994471_208994472insCT (hg19)
chr2:g.208129747_208129748insCT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.208129747_208129748insCT , CM000664.2:g.208129747_208129748insCT | GRCh38 |
| NC_000002.11:g.208994471_208994472insCT , CM000664.1:g.208994471_208994472insCT | GRCh37 |
| NC_000002.10:g.208702716_208702717insCT | NCBI36 |
| NG_008038.1:g.5083_5084insAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282141.4:c.9+36_9+37insAG MANE Select | ENSP00000282141.3:n.9+36_9+37insAG | |
| ENST00000282141.3:c.9+36_9+37insAG | ENSP00000282141.3:n.9+36_9+37insAG | |
| NM_020989.3:c.9+36_9+37insAG | NP_066269.1:n.9+36_9+37insAG | |
| NR_038437.1:n.98-7309_98-7308insCT | ||
| XM_011510661.1:c.9+36_9+37insAG | XP_011508963.1:n.9+36_9+37insAG | |
| XM_011510662.1:c.9+36_9+37insAG | XP_011508964.1:n.9+36_9+37insAG | |
| XM_011510663.1:c.-120-65_-120-64insAG | XP_011508965.1:n.-120-65_-120-64insAG | |
| NM_020989.4:c.9+36_9+37insAG MANE Select | NP_066269.1:n.9+36_9+37insAG |