Linked Data
gnomAD v4:
11-55812028-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.55812028G>T , CM000673.2:g.55812028G>T | GRCh38 |
| NC_000011.9:g.55579504G>T , CM000673.1:g.55579504G>T | GRCh37 |
| NC_000011.8:g.55336080G>T | NCBI36 |
| NG_052620.1:g.5662G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000625203.2:c.562G>T MANE Select | ENSP00000485319.1:p.Ala188Ser | |
| ENST00000333973.3:c.562G>T | ENSP00000335529.2:p.Ala188Ser | |
| ENST00000623450.1:c.562G>T | ENSP00000485509.1:p.Ala188Ser | |
| ENST00000625203.1:c.562G>T | ENSP00000485319.1:p.Ala188Ser | |
| NM_001004738.1:c.562G>T | NP_001004738.1:p.Ala188Ser | |
| NM_001004738.2:c.562G>T MANE Select | NP_001004738.1:p.Ala188Ser |