Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.186191803C= , CM000666.2:g.186191803C= | GRCh38 |
| NC_000004.11:g.187112957C= , CM000666.1:g.187112957C= | GRCh37 |
| NC_000004.10:g.187349951C= | NCBI36 |
| NG_007965.1:g.5284C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378802.5:c.-21C= MANE Select | ENSP00000368079.4:n.-21C= | |
| ENST00000378802.4:c.-21C= | ENSP00000368079.4:n.-21C= | |
| NM_207352.3:c.-21C= | NP_997235.3:n.-21C= | |
| XM_005262935.2:c.-21C= | XP_005262992.1:n.-21C= | |
| XM_005262935.4:c.-21C= | XP_005262992.1:n.-21C= | |
| XM_017008037.1:c.-331C= | XP_016863526.1:n.-331C= | |
| NM_207352.4:c.-21C= MANE Select | NP_997235.3:n.-21C= |