Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.30313958T>C , CM000672.2:g.30313958T>C | GRCh38 |
| NC_000010.10:g.30602887T>C , CM000672.1:g.30602887T>C | GRCh37 |
| NC_000010.9:g.30642893T>C | NCBI36 |
| NG_028096.1:g.40381A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263063.9:c.1400A>G MANE Select | ENSP00000263063.3:p.Asn467Ser | |
| ENST00000263063.8:c.1400A>G | ENSP00000263063.3:p.Asn467Ser | |
| ENST00000488290.5:n.3155A>G | ||
| NM_018109.3:c.1400A>G | NP_060579.3:p.Asn467Ser | |
| NM_018109.4:c.1400A>G MANE Select | NP_060579.3:p.Asn467Ser |