Linked Data
gnomAD v4:
10-30313518-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.30313518A>C , CM000672.2:g.30313518A>C | GRCh38 |
| NC_000010.10:g.30602447A>C , CM000672.1:g.30602447A>C | GRCh37 |
| NC_000010.9:g.30642453A>C | NCBI36 |
| NG_028096.1:g.40821T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263063.9:c.*91T>G MANE Select | ENSP00000263063.3:n.*91T>G | |
| ENST00000263063.8:c.*91T>G | ENSP00000263063.3:n.*91T>G | |
| ENST00000488290.5:n.3595T>G | ||
| NM_018109.3:c.*91T>G | NP_060579.3:n.*91T>G | |
| NM_018109.4:c.*91T>G MANE Select | NP_060579.3:n.*91T>G |