Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94775507G= , CM000672.2:g.94775507G= | GRCh38 |
| NC_000010.10:g.96535264G= , CM000672.1:g.96535264G= | GRCh37 |
| NC_000010.9:g.96525254G= | NCBI36 |
| NG_008384.2:g.17802G= | |
| NG_008384.3:g.17827G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.449G= MANE Select | ENSP00000360372.3:p.Arg150= | |
| ENST00000645461.1:n.1502G= | ||
| ENST00000371321.7:c.449G= | ENSP00000360372.3:p.Arg150= | |
| ENST00000464755.1:c.1212G= | ENSP00000483243.1:n.1212G= | |
| ENST00000480405.2:c.449G= | ENSP00000483847.1:p.Arg150= | |
| NM_000769.2:c.449G= | NP_000760.1:p.Arg150= | |
| NM_000769.4:c.449G= MANE Select | NP_000760.1:p.Arg150= |