Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.65979182A= , CM000673.2:g.65979182A= | GRCh38 |
| NC_000011.9:g.65746653A= , CM000673.1:g.65746653A= | GRCh37 |
| NC_000011.8:g.65503229A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000312397.10:c.*152A= MANE Select | ENSP00000310448.5:n.*152A= | |
| ENST00000312397.9:c.*152A= | ENSP00000310448.5:n.*152A= | |
| NM_005146.4:c.*152A= | NP_005137.1:n.*152A= | |
| XR_950099.3:n.2625A= | ||
| NM_005146.5:c.*152A= MANE Select | NP_005137.1:n.*152A= |