Linked Data
dbSNP Id:
rs1967970041
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713717_6713718insTT , CM000681.2:g.6713717_6713718insTT | GRCh38 |
| NC_000019.9:g.6713728_6713729insTT , CM000681.1:g.6713728_6713729insTT | GRCh37 |
| NC_000019.8:g.6664728_6664729insTT | NCBI36 |
| NG_009557.1:g.11934_11935insAA , LRG_27:g.11934_11935insAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.651-209_651-208insAA | ENSP00000512083.1:n.651-209_651-208insAA | |
| ENST00000245907.11:c.774-209_774-208insAA MANE Select | ENSP00000245907.4:n.774-209_774-208insAA | |
| ENST00000245907.10:c.774-209_774-208insAA | ENSP00000245907.4:n.774-209_774-208insAA | |
| ENST00000595577.1:n.278-209_278-208insAA | ||
| ENST00000597442.5:n.23+48_23+49insAA | ||
| NM_000064.3:c.774-209_774-208insAA | NP_000055.2:n.774-209_774-208insAA | |
| NM_000064.4:c.774-209_774-208insAA MANE Select | NP_000055.2:n.774-209_774-208insAA |