Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.78033760A= , CM000672.2:g.78033760A= | GRCh38 |
| NC_000010.10:g.79793518A= , CM000672.1:g.79793518A= | GRCh37 |
| NC_000010.9:g.79463524A= | NCBI36 |
| NG_012633.1:g.5001A= | |
| NG_029648.1:g.781T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613865.5:c.-142A= | ENSP00000478869.2:n.-142A= | |
| ENST00000435275.5:c.-142A= | ENSP00000415549.1:n.-142A= | |
| ENST00000440692.5:c.-142A= | ENSP00000414321.1:n.-142A= | |
| ENST00000613865.4:c.-142A= | ENSP00000478869.1:n.-142A= | |
| NM_001026.4:c.-142A= | NP_001017.1:n.-142A= | |
| NM_001142282.1:c.-142A= | NP_001135754.1:n.-142A= | |
| NM_001142283.1:c.-142A= | NP_001135755.1:n.-142A= | |
| NM_001142284.1:c.-142A= | NP_001135756.1:n.-142A= | |
| NM_001142285.1:c.-142A= | NP_001135757.1:n.-142A= | |
| NM_033022.3:c.-142A= | NP_148982.1:n.-142A= |