Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.177442492T= , CM000666.2:g.177442492T= | GRCh38 |
| NC_000004.11:g.178363646T= , CM000666.1:g.178363646T= | GRCh37 |
| NC_000004.10:g.178600640T= | NCBI36 |
| NG_011845.2:g.5012A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264595.6:c.-117A= | ENSP00000264595.2:n.-117A= | |
| NM_000027.3:c.-117A= | NP_000018.2:n.-117A= | |
| NM_001171988.1:c.-117A= | NP_001165459.1:n.-117A= | |
| NR_033655.1:n.12A= | ||
| XM_006714123.2:c.-117A= | XP_006714186.1:n.-117A= |