Linked Data
dbSNP Id:
rs1572774774
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21002308_21002309insT , CM000664.2:g.21002308_21002309insT | GRCh38 |
| NC_000002.11:g.21225180_21225181insT , CM000664.1:g.21225180_21225181insT | GRCh37 |
| NC_000002.10:g.21078685_21078686insT | NCBI36 |
| NG_011793.1:g.46765_46766insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.13113_13114insA MANE Select | ENSP00000233242.1:p.Gln4372ThrfsTer15 | |
| ENST00000616098.4:c.13111_13112insA | ENSP00000477990.1:n.13111_13112insA | |
| NM_000384.2:c.13113_13114insA | NP_000375.2:p.Gln4372ThrfsTer15 | |
| XM_011532809.1:c.5870-3036_5870-3035insA | XP_011531111.1:n.5870-3036_5870-3035insA | |
| NM_000384.3:c.13113_13114insA MANE Select | NP_000375.3:p.Gln4372ThrfsTer15 |