Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218893252G>C , CM000664.2:g.218893252G>C | GRCh38 |
| NC_000002.11:g.219757974G>C , CM000664.1:g.219757974G>C | GRCh37 |
| NC_000002.10:g.219466218G>C | NCBI36 |
| NG_012179.1:g.17720G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258411.8:c.1235G>C MANE Select | ENSP00000258411.3:p.Trp412Ser | |
| ENST00000258411.7:c.1235G>C | ENSP00000258411.3:p.Trp412Ser | |
| ENST00000489887.1:n.32G>C | ||
| NM_025216.2:c.1235G>C | NP_079492.2:p.Trp412Ser | |
| XM_011511928.1:c.1184G>C | XP_011510230.1:p.Trp395Ser | |
| XM_011511929.1:c.1139G>C | XP_011510231.1:p.Trp380Ser | |
| XM_011511930.1:c.855G>C | XP_011510232.1:p.Val285= | |
| XM_011511929.2:c.1139G>C | XP_011510231.1:p.Trp380Ser | |
| NM_025216.3:c.1235G>C MANE Select | NP_079492.2:p.Trp412Ser |