Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.23868000T>G , CM000663.2:g.23868000T>G | GRCh38 |
| NC_000001.10:g.24194490T>G , CM000663.1:g.24194490T>G | GRCh37 |
| NC_000001.9:g.24067077T>G | NCBI36 |
| NG_013346.1:g.5370A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374479.4:c.287A>C MANE Select | ENSP00000363603.3:p.Asn96Thr | |
| ENST00000374479.3:c.287A>C | ENSP00000363603.3:p.Asn96Thr | |
| NM_000147.4:c.287A>C | NP_000138.2:p.Asn96Thr | |
| XM_005245821.1:c.-263A>C | XP_005245878.1:n.-263A>C | |
| XM_005245821.3:c.-263A>C | XP_005245878.1:n.-263A>C | |
| NM_000147.5:c.287A>C MANE Select | NP_000138.2:p.Asn96Thr | |
| NR_174379.1:n.291A>C | ||
| NR_174380.1:n.291A>C | ||
| NR_174381.1:n.291A>C | ||
| NR_174382.1:n.291A>C |