Linked Data
gnomAD v4:
15-40931895-T-TC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40931895_40931896insC , CM000677.2:g.40931895_40931896insC | GRCh38 |
| NC_000015.9:g.41224093_41224094insC , CM000677.1:g.41224093_41224094insC | GRCh37 |
| NC_000015.8:g.39011385_39011386insC | NCBI36 |
| NG_046974.1:g.7563_7564insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249749.7:c.658+129_658+130insC MANE Select | ENSP00000249749.5:n.658+129_658+130insC | |
| ENST00000249749.6:c.658+129_658+130insC | ENSP00000249749.5:n.658+129_658+130insC | |
| ENST00000559440.1:n.887+129_887+130insC | ||
| NM_019074.3:c.658+129_658+130insC | NP_061947.1:n.658+129_658+130insC | |
| NM_019074.4:c.658+129_658+130insC MANE Select | NP_061947.1:n.658+129_658+130insC |