Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75004889C= , CM000676.2:g.75004889C= | GRCh38 |
| NC_000014.8:g.75471592C= , CM000676.1:g.75471592C= | GRCh37 |
| NC_000014.7:g.74541345C= | NCBI36 |
| NG_013333.1:g.6981C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266126.10:c.586C= MANE Select | ENSP00000266126.5:p.Pro196= | |
| ENST00000266126.9:c.586C= | ENSP00000266126.5:p.Pro196= | |
| ENST00000553401.5:c.559C= | ENSP00000451681.1:p.Pro187= | |
| ENST00000553539.1:n.881C= | ||
| ENST00000555522.1:n.644C= | ||
| ENST00000556028.5:c.586C= | ENSP00000452311.1:p.Pro196= | |
| NM_014239.3:c.586C= | NP_055054.1:p.Pro196= | |
| NM_014239.4:c.586C= MANE Select | NP_055054.1:p.Pro196= |