Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67583843C= , CM000673.2:g.67583843C= | GRCh38 |
| NC_000011.9:g.67351314C= , CM000673.1:g.67351314C= | GRCh37 |
| NC_000011.8:g.67107890C= | NCBI36 |
| NG_012075.1:g.5249C= , LRG_723:g.5249C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.-1C= | ENSP00000381604.1:n.-1C= | |
| ENST00000398606.10:c.-1C= MANE Select | ENSP00000381607.3:n.-1C= | |
| ENST00000646888.1:c.-1C= | ENSP00000494477.1:n.-1C= | |
| ENST00000398603.5:c.-1C= | ENSP00000381604.1:n.-1C= | |
| ENST00000398606.7:c.-1C= | ENSP00000381607.3:n.-1C= | |
| ENST00000494593.1:n.22C= | ||
| NM_000852.3:c.-1C= , LRG_723t1:c.-1C= | NP_000843.1:n.-1C= | |
| NM_000852.4:c.-1C= MANE Select | NP_000843.1:n.-1C= |