Linked Data
gnomAD v4:
11-61392357-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61392357G>T , CM000673.2:g.61392357G>T | GRCh38 |
| NC_000011.9:g.61159829G>T , CM000673.1:g.61159829G>T | GRCh37 |
| NC_000011.8:g.60916405G>T | NCBI36 |
| NG_032976.1:g.4998G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000515837.6:c.-275G>T | ENSP00000440638.1:n.-275G>T | |
| XM_005274039.3:c.-606G>T | XP_005274096.1:n.-606G>T | |
| XM_005274039.4:c.-606G>T | XP_005274096.1:n.-606G>T |