Linked Data
gnomAD v4:
16-1985866-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1985866G>T , CM000678.2:g.1985866G>T | GRCh38 |
| NC_000016.9:g.2035867G>T , CM000678.1:g.2035867G>T | GRCh37 |
| NC_000016.8:g.1975868G>T | NCBI36 |
| NG_016288.1:g.6718G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.231G>T | ENSP00000455885.1:p.Arg77Ser | |
| ENST00000248114.7:c.456G>T MANE Select | ENSP00000248114.6:p.Arg152Ser | |
| ENST00000248114.6:c.456G>T | ENSP00000248114.6:p.Arg152Ser | |
| ENST00000565658.1:n.613G>T | ||
| ENST00000567719.1:c.231G>T | ENSP00000455885.1:p.Arg77Ser | |
| ENST00000569451.1:c.259G>T | ENSP00000456432.1:p.Ala87Ser | |
| NM_005262.2:c.456G>T | NP_005253.3:p.Arg152Ser | |
| NM_005262.3:c.456G>T MANE Select | NP_005253.3:p.Arg152Ser |