Linked Data
gnomAD v4:
17-42404764-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42404764T>C , CM000679.2:g.42404764T>C | GRCh38 |
| NC_000017.10:g.40556782T>C , CM000679.1:g.40556782T>C | GRCh37 |
| NC_000017.9:g.37810308T>C | NCBI36 |
| NG_015845.1:g.23557A>G | |
| NG_015845.2:g.23557A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357037.6:c.1096A>G MANE Select | ENSP00000349541.4:p.Ser366Gly | |
| ENST00000357037.5:c.1096A>G | ENSP00000349541.4:p.Ser366Gly | |
| NM_012232.5:c.1096A>G | NP_036364.2:p.Ser366Gly | |
| NM_012232.6:c.1096A>G MANE Select | NP_036364.2:p.Ser366Gly |