Linked Data
gnomAD v4:
8-38145966-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38145966A>G , CM000670.2:g.38145966A>G | GRCh38 |
| NC_000008.10:g.38003484A>G , CM000670.1:g.38003484A>G | GRCh37 |
| NC_000008.9:g.38122641A>G | NCBI36 |
| NG_011827.1:g.10117T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000276449.9:c.647T>C MANE Select | ENSP00000276449.3:p.Ile216Thr | |
| ENST00000276449.8:c.647T>C | ENSP00000276449.3:p.Ile216Thr | |
| ENST00000520114.1:n.1134T>C | ||
| ENST00000522050.1:c.583T>C | ||
| NM_000349.2:c.647T>C | NP_000340.2:p.Ile216Thr | |
| XM_006716392.1:c.647T>C | XP_006716455.1:p.Ile216Thr | |
| NM_000349.3:c.647T>C MANE Select | NP_000340.2:p.Ile216Thr |