Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.140114667C= , CM000667.2:g.140114667C= | GRCh38 |
| NC_000005.9:g.139494252C= , CM000667.1:g.139494252C= | GRCh37 |
| NC_000005.8:g.139474436C= | NCBI36 |
| NG_041813.1:g.5545C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331327.5:c.486C= MANE Select | ENSP00000332706.3:p.Asn162= | |
| ENST00000651386.1:c.486C= | ENSP00000499133.1:p.Asn162= | |
| ENST00000331327.4:c.486C= | ENSP00000332706.3:p.Asn162= | |
| NM_005859.4:c.486C= | NP_005850.1:p.Asn162= | |
| NM_005859.5:c.486C= MANE Select | NP_005850.1:p.Asn162= |