Linked Data
gnomAD v4:
2-233618449-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.233618449A>T , CM000664.2:g.233618449A>T | GRCh38 |
| NC_000002.11:g.234527095A>T , CM000664.1:g.234527095A>T | GRCh37 |
| NC_000002.10:g.234191834A>T | NCBI36 |
| NG_002601.2:g.33706A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373450.5:c.742A>T MANE Select | ENSP00000362549.4:p.Thr248Ser | |
| ENST00000373450.4:c.742A>T | ENSP00000362549.4:p.Thr248Ser | |
| NM_019076.4:c.742A>T | NP_061949.3:p.Thr248Ser | |
| NM_019076.5:c.742A>T MANE Select | NP_061949.3:p.Thr248Ser |