Linked Data
gnomAD v4:
X-154896252-T-TG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154896252_154896253insG , CM000685.2:g.154896252_154896253insG | GRCh38 |
| NC_000023.10:g.154124527_154124528insG , CM000685.1:g.154124527_154124528insG | GRCh37 |
| NC_000023.9:g.153777721_153777722insG | NCBI36 |
| NG_011403.1:g.131471_131472insC | |
| NG_011403.2:g.131471_131472insC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.6274-21_6274-20insC MANE Select | ENSP00000353393.4:n.6274-21_6274-20insC | |
| ENST00000360256.8:c.6274-21_6274-20insC | ENSP00000353393.4:n.6274-21_6274-20insC | |
| NM_000132.3:c.6274-21_6274-20insC | NP_000123.1:n.6274-21_6274-20insC | |
| XM_011531126.1:c.6169-21_6169-20insC | XP_011529428.1:n.6169-21_6169-20insC | |
| NM_000132.4:c.6274-21_6274-20insC MANE Select | NP_000123.1:n.6274-21_6274-20insC |