Linked Data
gnomAD v4:
1-215675442-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215675442A>T , CM000663.2:g.215675442A>T | GRCh38 |
| NC_000001.10:g.215848784A>T , CM000663.1:g.215848784A>T | GRCh37 |
| NC_000001.9:g.213915407A>T | NCBI36 |
| NG_009497.1:g.752955T>A | |
| NG_009497.2:g.753007T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.12469T>A MANE Select | ENSP00000305941.3:p.Ser4157Thr | |
| ENST00000674083.1:c.12469T>A | ENSP00000501296.1:p.Ser4157Thr | |
| ENST00000307340.7:c.12469T>A | ENSP00000305941.3:p.Ser4157Thr | |
| NM_206933.2:c.12469T>A | NP_996816.2:p.Ser4157Thr | |
| NM_206933.3:c.12469T>A | NP_996816.2:p.Ser4157Thr | |
| NM_206933.4:c.12469T>A MANE Select | NP_996816.3:p.Ser4157Thr |