Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.18130781C= , CM000668.2:g.18130781C= | GRCh38 |
| NC_000006.11:g.18131012C= , CM000668.1:g.18131012C= | GRCh37 |
| NC_000006.10:g.18238991C= | NCBI36 |
| NG_012137.2:g.29363G= | |
| NG_012137.3:g.29363G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000367.5:c.626-1G= MANE Select | NP_000358.1:n.626-1G= |
| ENST00000309983.5:c.626-1G= MANE Select | ENSP00000312304.4:n.626-1G= |
| NM_000367.3:c.626-1G= | NP_000358.1:n.626-1G= |
| NM_000367.4:c.626-1G= | NP_000358.1:n.626-1G= |
| NM_001346817.1:c.626-1G= | NP_001333746.1:n.626-1G= |
| NM_001346818.1:c.581-1G= | NP_001333747.1:n.581-1G= |
| ENST00000309983.4:c.626-1G= | ENSP00000312304.4:n.626-1G= |
| XM_011514839.1:c.581-1G= | XP_011513141.1:n.581-1G= |
| XM_011514840.1:c.557-1G= | XP_011513142.1:n.557-1G= |