Linked Data
gnomAD v4:
17-61590778-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61590778C>A , CM000679.2:g.61590778C>A | GRCh38 |
| NC_000017.10:g.59668139C>A , CM000679.1:g.59668139C>A | GRCh37 |
| NC_000017.9:g.57022921C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000521764.3:c.403G>T MANE Select | ENSP00000427802.1:p.Ala135Ser | |
| ENST00000521764.2:c.403G>T | ENSP00000427802.1:p.Ala135Ser | |
| NM_199290.3:c.403G>T | NP_954984.1:p.Ala135Ser | |
| NM_199290.4:c.403G>T MANE Select | NP_954984.1:p.Ala135Ser |