Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52038265C= , CM000666.2:g.52038265C= | GRCh38 |
| NC_000004.11:g.52904431C= , CM000666.1:g.52904431C= | GRCh37 |
| NC_000004.10:g.52599188C= | NCBI36 |
| NG_008891.1:g.5055G= , LRG_204:g.5055G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.-6G= MANE Select | ENSP00000370839.6:n.-6G= | |
| ENST00000381431.9:c.-6G= | ENSP00000370839.5:n.-6G= | |
| NM_000232.4:c.-6G= , LRG_204t1:c.-6G= | NP_000223.1:n.-6G= | |
| XM_011534403.1:c.-6G= | XP_011532705.1:n.-6G= | |
| NM_000232.5:c.-6G= MANE Select | NP_000223.1:n.-6G= |