Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255626C= , CM000671.2:g.133255626C= | GRCh38 |
| NC_000009.11:g.136131013C= , CM000671.1:g.136131013C= | GRCh37 |
| NC_000009.10:g.135120834C= | NCBI36 |
| NG_006669.1:g.22042G= | |
| NG_006669.2:g.24590G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.1134G= | ||
| ENST00000647353.1:n.54-4474G= | ||
| ENST00000679909.1:c.28+19536G= | ENSP00000506089.1:n.28+19536G= | |
| ENST00000453660.3:n.1116G= | ||
| ENST00000538324.2:c.1098G= | ENSP00000483018.1:p.Pro366= | |
| ENST00000611156.4:c.*40G= | ENSP00000483265.1:n.*40G= | |
| NM_020469.2:c.*40G= | NP_065202.2:n.*40G= | |
| NM_020469.3:c.*40G= | NP_065202.2:n.*40G= |