Linked Data
dbSNP Id:
rs2121101339
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21174732_21174733insAC , CM000674.2:g.21174732_21174733insAC | GRCh38 |
| NC_000012.11:g.21327666_21327667insAC , CM000674.1:g.21327666_21327667insAC | GRCh37 |
| NC_000012.10:g.21218933_21218934insAC | NCBI36 |
| NG_011745.1:g.48539_48540insAC , LRG_1022:g.48539_48540insAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.359+23_359+24insAC MANE Select | ENSP00000256958.2:n.359+23_359+24insAC | |
| ENST00000256958.2:c.359+23_359+24insAC | ENSP00000256958.2:n.359+23_359+24insAC | |
| ENST00000543498.5:c.426-2044_426-2043insAC | ||
| NM_006446.4:c.359+23_359+24insAC , LRG_1022t1:c.359+23_359+24insAC | NP_006437.3:n.359+23_359+24insAC | |
| NM_006446.5:c.359+23_359+24insAC MANE Select | NP_006437.3:n.359+23_359+24insAC |