Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.3518075C>G , CM000666.2:g.3518075C>G | GRCh38 |
| NC_000004.11:g.3519802C>G , CM000666.1:g.3519802C>G | GRCh37 |
| NC_000004.10:g.3489600C>G | NCBI36 |
| NG_033873.1:g.19423G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648517.1:c.710G>C | ENSP00000496947.1:p.Arg237Pro | |
| ENST00000650182.1:c.710G>C MANE Select | ENSP00000497444.1:p.Arg237Pro | |
| ENST00000296325.9:n.673G>C | ||
| ENST00000500728.2:c.710G>C | ENSP00000421922.1:p.Arg237Pro | |
| ENST00000509198.1:n.756G>C | ||
| ENST00000515119.5:c.*487G>C | ENSP00000421648.1:n.*487G>C | |
| NM_002337.3:c.710G>C | NP_002328.1:p.Arg237Pro | |
| NR_110005.1:n.673G>C | ||
| NM_002337.4:c.710G>C MANE Select | NP_002328.1:p.Arg237Pro | |
| XR_002959730.1:n.795G>C | ||
| NR_110005.2:n.673G>C |