Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.37805034G>C , CM000685.2:g.37805034G>C | GRCh38 |
| NC_000023.10:g.37664287G>C , CM000685.1:g.37664287G>C | GRCh37 |
| NC_000023.9:g.37549231G>C | NCBI36 |
| NG_009065.1:g.30018G>C , LRG_53:g.30018G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696170.1:c.*689G>C | ENSP00000512461.1:n.*689G>C | |
| ENST00000696171.1:c.1084G>C | ENSP00000512462.1:p.Ala362Pro | |
| ENST00000378588.5:c.1180G>C MANE Select | ENSP00000367851.4:p.Ala394Pro | |
| ENST00000378588.4:c.1180G>C | ENSP00000367851.4:p.Ala394Pro | |
| ENST00000465127.1:c.171+379034G>C | ENSP00000417050.1:n.171+379034G>C | |
| NM_000397.3:c.1180G>C , LRG_53t1:c.1180G>C | NP_000388.2:p.Ala394Pro | |
| XM_011543890.1:c.874G>C | XP_011542192.1:p.Ala292Pro | |
| NM_000397.4:c.1180G>C MANE Select | NP_000388.2:p.Ala394Pro |