Linked Data
gnomAD v4:
20-10673534-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10673534T>G , CM000682.2:g.10673534T>G | GRCh38 |
| NC_000020.10:g.10654182T>G , CM000682.1:g.10654182T>G | GRCh37 |
| NC_000020.9:g.10602182T>G | NCBI36 |
| NG_007496.1:g.5513A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.-4A>C MANE Select | ENSP00000254958.4:n.-4A>C | |
| ENST00000254958.9:c.-4A>C | ENSP00000254958.4:n.-4A>C | |
| NM_000214.2:c.-4A>C | NP_000205.1:n.-4A>C | |
| NM_000214.3:c.-4A>C MANE Select | NP_000205.1:n.-4A>C |