Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232542288T= , CM000664.2:g.232542288T= | GRCh38 |
| NC_000002.11:g.233406998T= , CM000664.1:g.233406998T= | GRCh37 |
| NC_000002.10:g.233115242T= | NCBI36 |
| NG_012954.1:g.7562T= | |
| NG_012954.2:g.7597T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005199.5:c.507-135T= MANE Select | NP_005190.4:n.507-135T= |
| ENST00000651502.1:c.507-135T= MANE Select | ENSP00000498757.1:n.507-135T= |
| NM_005199.4:c.507-135T= | NP_005190.4:n.507-135T= |
| ENST00000389492.3:c.351-135T= | ENSP00000374143.3:n.351-135T= |
| ENST00000389494.7:c.507-135T= | ENSP00000374145.3:n.507-135T= |