Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47403118A= , CM000664.2:g.47403118A= | GRCh38 |
| NC_000002.11:g.47630257A= , CM000664.1:g.47630257A= | GRCh37 |
| NC_000002.10:g.47483761A= | NCBI36 |
| NG_007110.2:g.4995A= , LRG_218:g.4995A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000543555.6:c.-88A= | ENSP00000442697.1:n.-88A= | |
| ENST00000233146.6:c.-74A= | ENSP00000233146.2:n.-74A= | |
| ENST00000454849.5:c.-88A= | ENSP00000411482.1:n.-88A= | |
| ENST00000543555.5:c.-88A= | ENSP00000442697.1:n.-88A= | |
| NM_000251.2:c.-74A= , LRG_218t1:c.-74A= | NP_000242.1:n.-74A= | |
| NM_001258281.1:c.-88A= | NP_001245210.1:n.-88A= |