Linked Data
gnomAD v4:
16-1986037-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1986037C>T , CM000678.2:g.1986037C>T | GRCh38 |
| NC_000016.9:g.2036038C>T , CM000678.1:g.2036038C>T | GRCh37 |
| NC_000016.8:g.1976039C>T | NCBI36 |
| NG_016288.1:g.6889C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.*9C>T | ENSP00000455885.1:n.*9C>T | |
| ENST00000248114.7:c.*9C>T MANE Select | ENSP00000248114.6:n.*9C>T | |
| ENST00000248114.6:c.*9C>T | ENSP00000248114.6:n.*9C>T | |
| ENST00000565658.1:n.784C>T | ||
| ENST00000567719.1:c.*9C>T | ENSP00000455885.1:n.*9C>T | |
| ENST00000569451.1:c.*100C>T | ENSP00000456432.1:n.*100C>T | |
| NM_005262.2:c.*9C>T | NP_005253.3:n.*9C>T | |
| NM_005262.3:c.*9C>T MANE Select | NP_005253.3:n.*9C>T |