Linked Data
gnomAD v4:
12-5044854-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.5044854T>C , CM000674.2:g.5044854T>C | GRCh38 |
| NC_000012.11:g.5154020T>C , CM000674.1:g.5154020T>C | GRCh37 |
| NC_000012.10:g.5024281T>C | NCBI36 |
| NG_012198.1:g.5936T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252321.5:c.707T>C MANE Select | ENSP00000252321.3:p.Val236Ala | |
| ENST00000252321.4:c.707T>C | ENSP00000252321.3:p.Val236Ala | |
| NM_002234.3:c.707T>C | NP_002225.2:p.Val236Ala | |
| NM_002234.4:c.707T>C MANE Select | NP_002225.2:p.Val236Ala |