Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.27085180G= , CM000664.2:g.27085180G= | GRCh38 |
| NC_000002.11:g.27308048G= , CM000664.1:g.27308048G= | GRCh37 |
| NC_000002.10:g.27161552G= | NCBI36 |
| NG_012199.1:g.3438G= | |
| NG_046849.1:g.11614G= | |
| NG_012199.2:g.3438G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380320.9:c.2596G= MANE Select | ENSP00000369677.4:p.Ala866= | |
| ENST00000380320.8:c.2596G= | ENSP00000369677.4:p.Ala866= | |
| ENST00000433140.1:c.588G= | ||
| NM_007046.3:c.2596G= | NP_008977.1:p.Ala866= | |
| XM_006711928.2:c.2575+172G= | XP_006711991.1:n.2575+172G= | |
| NM_007046.4:c.2596G= MANE Select | NP_008977.1:p.Ala866= |