Linked Data
gnomAD v4:
19-47003914-A-ACG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.47003915_47003916insGC , CM000681.2:g.47003915_47003916insGC | GRCh38 |
| NC_000019.9:g.47507172_47507173insGC , CM000681.1:g.47507172_47507173insGC | GRCh37 |
| NC_000019.8:g.52199012_52199013insGC | NCBI36 |
| NG_047014.1:g.90349_90350insGC | |
| NG_047014.2:g.147919_147920insGC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000404338.8:c.7727_7728insGC | ENSP00000385720.2:n.7727_7728insGC | |
| ENST00000672722.1:c.*3227_*3228insGC MANE Select | ENSP00000500409.1:n.*3227_*3228insGC | |
| ENST00000404338.7:c.7727_7728insGC | ENSP00000385720.2:n.7727_7728insGC | |
| ENST00000614079.1:c.7304_7305insGC | ENSP00000483730.1:n.7304_7305insGC | |
| NM_004491.4:c.7727_7728insGC | NP_004482.4:n.7727_7728insGC | |
| NM_004491.5:c.*3227_*3228insGC MANE Select | NP_004482.4:n.*3227_*3228insGC |