Linked Data
gnomAD v4:
1-53196651-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.53196651C>T , CM000663.2:g.53196651C>T | GRCh38 |
| NC_000001.10:g.53662323C>T , CM000663.1:g.53662323C>T | GRCh37 |
| NC_000001.9:g.53434911C>T | NCBI36 |
| NG_008035.1:g.5223C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371486.3:c.-293C>T | ENSP00000360541.3:n.-293C>T | |
| NM_000098.2:c.-293C>T | NP_000089.1:n.-293C>T | |
| NM_001330589.1:c.-293C>T | NP_001317518.1:n.-293C>T |