Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67940443T>G , CM000678.2:g.67940443T>G | GRCh38 |
| NC_000016.9:g.67974346T>G , CM000678.1:g.67974346T>G | GRCh37 |
| NC_000016.8:g.66531847T>G | NCBI36 |
| NG_009778.1:g.8670A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.784A>C MANE Select | ENSP00000264005.5:p.Lys262Gln | |
| ENST00000264005.9:c.784A>C | ENSP00000264005.5:p.Lys262Gln | |
| ENST00000570369.5:c.156-369A>C | ||
| ENST00000570980.1:c.568A>C | ENSP00000464651.1:p.Lys190Gln | |
| ENST00000573538.5:c.522A>C | ENSP00000463220.1:n.522A>C | |
| NM_000229.1:c.784A>C | NP_000220.1:p.Lys262Gln | |
| NM_000229.2:c.784A>C MANE Select | NP_000220.1:p.Lys262Gln |