Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255770G= , CM000671.2:g.133255770G= | GRCh38 |
| NC_000009.11:g.136131157G= , CM000671.1:g.136131157G= | GRCh37 |
| NC_000009.10:g.135120978G= | NCBI36 |
| NG_006669.1:g.21898C= | |
| NG_006669.2:g.24446C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.990C= | ||
| ENST00000647353.1:n.54-4618C= | ||
| ENST00000679909.1:c.28+19392C= | ENSP00000506089.1:n.28+19392C= | |
| ENST00000453660.3:n.972C= | ||
| ENST00000538324.2:c.958C= | ENSP00000483018.1:p.Pro320= | |
| ENST00000611156.4:c.958C= | ENSP00000483265.1:p.Pro320= | |
| NM_020469.2:c.961C= | NP_065202.2:p.Pro321= | |
| NM_020469.3:c.961C= | NP_065202.2:p.Pro321= |