Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133257947T= , CM000671.2:g.133257947T= | GRCh38 |
| NC_000009.11:g.136133334T= , CM000671.1:g.136133334T= | GRCh37 |
| NC_000009.10:g.135123155T= | NCBI36 |
| NG_006669.1:g.19720A= | |
| NG_006669.2:g.22268A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.269+150A= | ||
| ENST00000647353.1:n.54-6795A= | ||
| ENST00000651471.1:n.329+95A= | ||
| ENST00000679909.1:c.28+17215A= | ENSP00000506089.1:n.28+17215A= | |
| ENST00000453660.3:n.251+150A= | ||
| ENST00000538324.2:c.239+150A= | ENSP00000483018.1:n.239+150A= | |
| ENST00000611156.4:c.239+150A= | ENSP00000483265.1:n.239+150A= | |
| NM_020469.2:c.239+150A= | NP_065202.2:n.239+150A= | |
| NM_020469.3:c.239+150A= | NP_065202.2:n.239+150A= |