Linked Data
gnomAD v4:
12-48981793-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48981793A>C , CM000674.2:g.48981793A>C | GRCh38 |
| NC_000012.11:g.49375576A>C , CM000674.1:g.49375576A>C | GRCh37 |
| NC_000012.10:g.47661843A>C | NCBI36 |
| NG_033141.1:g.8341A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293549.4:c.*153A>C MANE Select | ENSP00000293549.3:n.*153A>C | |
| NM_005430.3:c.*153A>C | NP_005421.1:n.*153A>C | |
| NM_005430.4:c.*153A>C MANE Select | NP_005421.1:n.*153A>C |