Linked Data
gnomAD v4:
10-30313470-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.30313470A>T , CM000672.2:g.30313470A>T | GRCh38 |
| NC_000010.10:g.30602399A>T , CM000672.1:g.30602399A>T | GRCh37 |
| NC_000010.9:g.30642405A>T | NCBI36 |
| NG_028096.1:g.40869T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263063.9:c.*139T>A MANE Select | ENSP00000263063.3:n.*139T>A | |
| ENST00000263063.8:c.*139T>A | ENSP00000263063.3:n.*139T>A | |
| ENST00000488290.5:n.3643T>A | ||
| NM_018109.3:c.*139T>A | NP_060579.3:n.*139T>A | |
| NM_018109.4:c.*139T>A MANE Select | NP_060579.3:n.*139T>A |