Linked Data
gnomAD v4:
9-21140678-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.21140678T>G , CM000671.2:g.21140678T>G | GRCh38 |
| NC_000009.11:g.21140677T>G , CM000671.1:g.21140677T>G | GRCh37 |
| NC_000009.10:g.21130677T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000380229.4:c.*305A>C MANE Select | ENSP00000369578.2:n.*305A>C | |
| ENST00000380229.3:c.*305A>C | ENSP00000369578.2:n.*305A>C | |
| NM_002177.1:c.*305A>C | NP_002168.1:n.*305A>C | |
| NM_002177.2:c.*305A>C | NP_002168.1:n.*305A>C | |
| NM_002177.3:c.*305A>C MANE Select | NP_002168.1:n.*305A>C |