Linked Data
gnomAD v4:
12-48981792-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48981792T>C , CM000674.2:g.48981792T>C | GRCh38 |
| NC_000012.11:g.49375575T>C , CM000674.1:g.49375575T>C | GRCh37 |
| NC_000012.10:g.47661842T>C | NCBI36 |
| NG_033141.1:g.8340T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293549.4:c.*152T>C MANE Select | ENSP00000293549.3:n.*152T>C | |
| NM_005430.3:c.*152T>C | NP_005421.1:n.*152T>C | |
| NM_005430.4:c.*152T>C MANE Select | NP_005421.1:n.*152T>C |