Linked Data
dbSNP Id:
rs1279127212
MyVariant Identifiers:
chr9:g.136130779_136130780insTGTGTG (hg19)
chr9:g.133255392_133255393insTGTGTG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255396_133255401dup , CM000671.2:g.133255396_133255401dup | GRCh38 |
| NC_000009.11:g.136130783_136130788dup , CM000671.1:g.136130783_136130788dup | GRCh37 |
| NC_000009.10:g.135120604_135120609dup | NCBI36 |
| NG_006669.1:g.22270_22275dup | |
| NG_006669.2:g.24818_24823dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.1362_1367dup | ||
| ENST00000647353.1:n.54-4246_54-4241dup | ||
| ENST00000679909.1:c.28+19764_28+19769dup | ENSP00000506089.1:n.28+19764_28+19769dup | |
| ENST00000453660.3:n.1344_1349dup | ||
| ENST00000611156.4:c.*268_*273dup | ENSP00000483265.1:n.*268_*273dup | |
| NM_020469.2:c.*268_*273dup | NP_065202.2:n.*268_*273dup | |
| NM_020469.3:c.*268_*273dup | NP_065202.2:n.*268_*273dup |