Linked Data
dbSNP Id:
rs1663001127
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21002197_21002198insC , CM000664.2:g.21002197_21002198insC | GRCh38 |
| NC_000002.11:g.21225069_21225070insC , CM000664.1:g.21225069_21225070insC | GRCh37 |
| NC_000002.10:g.21078574_21078575insC | NCBI36 |
| NG_011793.1:g.46876_46877insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.13224_13225insG MANE Select | ENSP00000233242.1:p.Ser4409GlufsTer11 | |
| ENST00000616098.4:c.13222_13223insG | ENSP00000477990.1:n.13222_13223insG | |
| NM_000384.2:c.13224_13225insG | NP_000375.2:p.Ser4409GlufsTer11 | |
| XM_011532809.1:c.5870-2925_5870-2924insG | XP_011531111.1:n.5870-2925_5870-2924insG | |
| NM_000384.3:c.13224_13225insG MANE Select | NP_000375.3:p.Ser4409GlufsTer11 |