Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.31667278A>C , CM000683.2:g.31667278A>C | GRCh38 |
| NC_000021.8:g.33039591A>C , CM000683.1:g.33039591A>C | GRCh37 |
| NC_000021.7:g.31961462A>C | NCBI36 |
| NG_008689.1:g.12657A>C , LRG_652:g.12657A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270142.11:c.260A>C MANE Select | ENSP00000270142.7:p.Asn87Thr | |
| ENST00000270142.10:c.260A>C | ENSP00000270142.6:p.Asn87Thr | |
| ENST00000389995.4:c.203A>C | ENSP00000374645.4:p.Asn68Thr | |
| ENST00000470944.1:n.1188A>C | ||
| ENST00000476106.5:n.523A>C | ||
| NM_000454.4:c.260A>C , LRG_652t1:c.260A>C | NP_000445.1:p.Asn87Thr | |
| NM_000454.5:c.260A>C MANE Select | NP_000445.1:p.Asn87Thr |