Linked Data
gnomAD v4:
17-4898792-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4898792C>G , CM000679.2:g.4898792C>G | GRCh38 |
| NC_000017.10:g.4802087C>G , CM000679.1:g.4802087C>G | GRCh37 |
| NC_000017.9:g.4742866C>G | NCBI36 |
| NG_008029.2:g.9284G>C | |
| NG_028005.1:g.70453C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649488.2:c.1426G>C MANE Select | ENSP00000497829.1:p.Gly476Arg | |
| ENST00000649830.1:c.*62G>C | ENSP00000496907.1:n.*62G>C | |
| ENST00000652550.1:n.1152G>C | ||
| ENST00000293780.4:c.1426G>C | ENSP00000293780.4:p.Gly476Arg | |
| ENST00000572438.1:n.1112G>C | ||
| NM_000080.3:c.1426G>C | NP_000071.1:p.Gly476Arg | |
| NM_000080.4:c.1426G>C MANE Select | NP_000071.1:p.Gly476Arg | |
| XM_017024115.1:c.1390G>C | XP_016879604.1:p.Gly464Arg |