Linked Data
dbSNP Id:
rs1663315451
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21011341_21011342insAA , CM000664.2:g.21011341_21011342insAA | GRCh38 |
| NC_000002.11:g.21234213_21234214insAA , CM000664.1:g.21234213_21234214insAA | GRCh37 |
| NC_000002.10:g.21087718_21087719insAA | NCBI36 |
| NG_011793.1:g.37733_37734insTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.5527_5528insTT MANE Select | ENSP00000233242.1:p.Ser1843PhefsTer? | |
| ENST00000616098.4:c.5527_5528insTT | ENSP00000477990.1:p.Ser1843PhefsTer? | |
| NM_000384.2:c.5527_5528insTT | NP_000375.2:p.Ser1843PhefsTer? | |
| XM_011532809.1:c.5527_5528insTT | XP_011531111.1:p.Ser1843PhefsTer? | |
| NM_000384.3:c.5527_5528insTT MANE Select | NP_000375.3:p.Ser1843PhefsTer? |