Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133260313C>T , CM000671.2:g.133260313C>T | GRCh38 |
| NC_000009.11:g.136135716C>T , CM000671.1:g.136135716C>T | GRCh37 |
| NC_000009.10:g.135125537C>T | NCBI36 |
| NG_006669.1:g.17337G>A | |
| NG_006669.2:g.19902G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.186-447G>A | ||
| ENST00000647353.1:n.54-9161G>A | ||
| ENST00000651471.1:n.191-447G>A | ||
| ENST00000679909.1:c.28+14849G>A | ENSP00000506089.1:n.28+14849G>A | |
| ENST00000453660.3:n.168-447G>A | ||
| ENST00000538324.2:c.156-447G>A | ENSP00000483018.1:n.156-447G>A | |
| ENST00000611156.4:c.156-447G>A | ENSP00000483265.1:n.156-447G>A | |
| NM_020469.2:c.156-447G>A | NP_065202.2:n.156-447G>A | |
| NM_020469.3:c.156-447G>A | NP_065202.2:n.156-447G>A |