Linked Data
gnomAD v4:
13-27924562-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924562T>C , CM000675.2:g.27924562T>C | GRCh38 |
| NC_000013.10:g.28498699T>C , CM000675.1:g.28498699T>C | GRCh37 |
| NC_000013.9:g.27396699T>C | NCBI36 |
| NG_008183.1:g.9532T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.713T>C MANE Select | ENSP00000370421.4:p.Leu238Pro | |
| ENST00000381033.4:c.713T>C | ENSP00000370421.4:p.Leu238Pro | |
| NM_000209.3:c.713T>C | NP_000200.1:p.Leu238Pro | |
| NM_000209.4:c.713T>C MANE Select | NP_000200.1:p.Leu238Pro |