Linked Data
gnomAD v4:
12-5043942-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5043942T>C , CM000674.2:g.5043942T>C | GRCh38 |
| NC_000012.11:g.5153108T>C , CM000674.1:g.5153108T>C | GRCh37 |
| NC_000012.10:g.5023369T>C | NCBI36 |
| NG_012198.1:g.5024T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.-206T>C MANE Select | ENSP00000252321.3:n.-206T>C | |
| NM_002234.3:c.-206T>C | NP_002225.2:n.-206T>C | |
| NM_002234.4:c.-206T>C MANE Select | NP_002225.2:n.-206T>C |