Linked Data
gnomAD v4:
8-37965689-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37965689C>T , CM000670.2:g.37965689C>T | GRCh38 |
| NC_000008.10:g.37823207C>T , CM000670.1:g.37823207C>T | GRCh37 |
| NC_000008.9:g.37942364C>T | NCBI36 |
| NG_011936.1:g.5978G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000345060.5:c.781G>A MANE Select | ENSP00000343782.3:p.Ala261Thr | |
| ENST00000520341.2:n.909G>A | ||
| ENST00000647937.1:c.265G>A | ENSP00000497740.1:p.Ala89Thr | |
| ENST00000345060.4:c.781G>A | ENSP00000343782.3:p.Ala261Thr | |
| ENST00000520341.1:n.56G>A | ||
| ENST00000614635.1:c.781G>A | ENSP00000480325.1:p.Ala261Thr | |
| NM_000025.2:c.781G>A | NP_000016.1:p.Ala261Thr | |
| NM_000025.3:c.781G>A MANE Select | NP_000016.1:p.Ala261Thr |