Linked Data
gnomAD v4:
16-30993216-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30993216A>G , CM000678.2:g.30993216A>G | GRCh38 |
| NC_000016.9:g.31004537A>G , CM000678.1:g.31004537A>G | GRCh37 |
| NC_000016.8:g.30912038A>G | NCBI36 |
| NG_041829.1:g.22293T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215095.11:c.700T>C MANE Select | ENSP00000215095.5:p.Tyr234His | |
| ENST00000565419.2:c.700T>C | ENSP00000455899.1:p.Tyr234His | |
| ENST00000215095.9:c.700T>C | ENSP00000215095.5:p.Tyr234His | |
| ENST00000565419.1:c.700T>C | ENSP00000455899.1:p.Tyr234His | |
| ENST00000569638.5:c.448T>C | ENSP00000457067.1:p.Tyr150His | |
| NM_052874.4:c.700T>C | NP_443106.1:p.Tyr234His | |
| XM_017022893.1:c.682T>C | XP_016878382.1:p.Tyr228His | |
| NM_052874.5:c.700T>C MANE Select | NP_443106.1:p.Tyr234His |