Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63038961C= , CM000670.2:g.63038961C= | GRCh38 |
| NC_000008.10:g.63951520C= , CM000670.1:g.63951520C= | GRCh37 |
| NC_000008.9:g.64114074C= | NCBI36 |
| NG_028126.1:g.5091G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000677327.1:n.447G= | ||
| ENST00000679326.1:c.-193G= | ENSP00000504262.1:n.-193G= | |
| ENST00000260118.6:c.-193G= | ENSP00000260118.6:n.-193G= | |
| NM_003878.2:c.-193G= | NP_003869.1:n.-193G= | |
| XM_011517623.1:c.-193G= | XP_011515925.1:n.-193G= |