Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.112782545C= , CM000664.2:g.112782545C= | GRCh38 |
| NC_000002.11:g.113540122C= , CM000664.1:g.113540122C= | GRCh37 |
| NC_000002.10:g.113256593C= | NCBI36 |
| NG_008850.1:g.7850G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000263339.4:c.96+171G= MANE Select | ENSP00000263339.3:n.96+171G= | |
| ENST00000263339.3:c.96+171G= | ENSP00000263339.3:n.96+171G= | |
| NM_000575.3:c.96+171G= | NP_000566.3:n.96+171G= | |
| NM_000575.4:c.96+171G= | NP_000566.3:n.96+171G= | |
| NM_000575.5:c.96+171G= MANE Select | NP_000566.3:n.96+171G= | |
| NM_001371554.1:c.96+171G= | NP_001358483.1:n.96+171G= |