Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.74789170G= , CM000669.2:g.74789170G= | GRCh38 |
| NC_000007.13:g.74203514G= , CM000669.1:g.74203514G= | GRCh37 |
| NC_000007.12:g.73841450G= | NCBI36 |
| NG_009078.2:g.20207G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289473.11:c.*10G= MANE Select | ENSP00000289473.4:n.*10G= | |
| ENST00000289473.10:c.*10G= | ENSP00000289473.4:n.*10G= | |
| ENST00000289473.8:c.*10G= | ENSP00000289473.4:n.*10G= | |
| ENST00000398421.6:n.2210G= | ||
| ENST00000455062.2:n.1292G= | ||
| NM_000265.5:c.*10G= | NP_000256.4:n.*10G= | |
| XM_005250543.3:c.*104G= | XP_005250600.2:n.*104G= | |
| XM_011516498.1:c.*57G= | XP_011514800.1:n.*57G= | |
| XM_011516501.1:c.*10G= | XP_011514803.1:n.*10G= | |
| NM_000265.6:c.*10G= | NP_000256.4:n.*10G= | |
| NM_000265.7:c.*10G= MANE Select | NP_000256.4:n.*10G= |