Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67584731A>C , CM000673.2:g.67584731A>C | GRCh38 |
| NC_000011.9:g.67352202A>C , CM000673.1:g.67352202A>C | GRCh37 |
| NC_000011.8:g.67108778A>C | NCBI36 |
| NG_012075.1:g.6137A>C , LRG_723:g.6137A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.191A>C | ENSP00000381604.1:p.Tyr64Ser | |
| ENST00000398606.10:c.191A>C MANE Select | ENSP00000381607.3:p.Tyr64Ser | |
| ENST00000646888.1:c.84A>C | ENSP00000494477.1:p.Val28= | |
| ENST00000398603.5:c.191A>C | ENSP00000381604.1:p.Tyr64Ser | |
| ENST00000398606.7:c.191A>C | ENSP00000381607.3:p.Tyr64Ser | |
| ENST00000489040.1:n.190A>C | ||
| ENST00000494593.1:n.621A>C | ||
| ENST00000498765.5:c.154A>C | ||
| NM_000852.3:c.191A>C , LRG_723t1:c.191A>C | NP_000843.1:p.Tyr64Ser | |
| NM_000852.4:c.191A>C MANE Select | NP_000843.1:p.Tyr64Ser |